Smart hydrogel particles for biomarker harvesting

ABSTRACT

Capture particles for harvesting analytes from solution and methods for using them are described. The capture particles are made up of a polymeric matrix having pore size that allows for the analytes to enter the capture particles. The pore size of the capture particles are changeable upon application of a stimulus to the particles, allowing the pore size of the particles to be changed so that analytes of interest remain sequestered inside the particles. The polymeric matrix of the capture particles are made of co-polymeric materials having a structural monomer and an affinity monomer, the affinity monomer having properties that attract the analyte to the capture particle. The capture particles may be used to isolate and identify analytes present in a mixture. They may also be used to protect analytes which are typically subject to degradation upon harvesting and to concentrate low an analyte in low abundance in a fluid.

STATEMENT OF PRIORITY

This application claims priority to U.S. Provisional Patent Application Ser. No. 60/986,803, filed Nov. 9, 2007, and is a continuation-in-part of U.S. patent application Ser. No. 11/527,727, filed Sep. 27, 2006, and is a continuation-in part of U.S. Utility patent application Ser. No. 12/033,701, filed Feb. 19, 2008, the disclosures of which are hereby incorporated by reference herein.

FIELD OF THE INVENTION

The present invention relates to particles for the harvesting of biomarkers from a mixture as well as methods for using the particles. More specifically, the present invention relates to particles capable of sequestering a biomarker from a mixture, allowing for the separation of the biomarker from the mixture, as well as methods for sequestering biomarkers. The present invention further denotes core-shell hydrogel particles having been synthesized and successfully applied to harvest, concentrate, and protect from degradation, a low abundance labile clinical biomarker from serum, a known complex biologic fluid targeted for biomarker discovery.

BACKGROUND OF THE INVENTION

Biomarkers can provide for early stage detection of a wide variety of diseases. As such, there is an urgent need to discover novel biomarkers that provide sensitive and specific disease detection (Aebersold et al., Proteome Res 2005, 4, (4), 1104-9; Srinivas et al., Clin Chem 2002, 48, (8), 1160-9). Biomarkers provide a way to diagnose a disease before clinical pathologies appear, allowing for early stage treatment of the disease, which typically provides better results.

For example, cancer is rapidly becoming the leading cause of death for many population groups in the United States, largely due to the fact that various types of the disease are usually diagnosed after the cancer has metastasized. At this later stage of the disease, treatment is typically invasive and ineffective. It is widely believed that early detection of cancer prior to metastasis will lead to a dramatic improvement in treatment outcome.

Biomarkers are also continually being discovered that are indicative of various other disease states and conditions as varied as Alzheimer's disease and diabetes. For many of these diseases, the early diagnosis of the disease allows for treatment options that have a greater chance of success than late stage treatment. Further, in some cases, early diagnosis of a disease or predisposition to a disease may even allow the person diagnosed to make lifestyle changes that may help to prevent and reverse the course of the disease without the need for more involved medical treatment.

Biomarkers are nucleic acids, proteins, protein fragments or metabolites indicative of a specific biological state, that are associated with the risk of contraction or presence of disease (Frank and Hargreaves; Nature reviews 2003, 2, (7), 566-80). Biomarker research has revealed that low-abundance circulating proteins and peptides present a rich source of information regarding the state of the organism as a whole (Esp in a et ai. Proteomics 2003, 3, (11), 2091-100). Two major hurdles have prevented these discoveries from reaching clinical benefit: 1) disease-relevant biomarkers in blood or body fluids may exist in exceedingly low concentrations within a complex mixture of biomolecules and could be masked by high-abundance species such as albumin, and 2) degradation of protein biomarkers can occur immediately following the collection of blood or body fluid as a result of endogenous or exogenous proteinases.

The concentration of proteins and peptides comprising the complex circulatory proteome ranges from 10-12 mg/mL to 10-3 mg/mL, spanning ten orders of magnitude, with a few high molecular weight proteins such as albumin and immunoglobulins accounting for 90% of total protein content (Anderson and Anderson, Mol Cell Proteomics 2002, 1, (11), 845-67). However, the low abundance and low molecular weight proteins and metabolites also present in the blood provide a wealth of information and have great promise as a source of new biomarkers. Conventional methods, such as two dimensional gel electrophoresis, do not have the sensitivity and resolution to detect and quantify low abundance low molecular weight proteins and metabolites. Also, in spite of the moderately high sensitivity of modem mass spectrometers (attomolar concentration), their working range spans over three-four orders of magnitude and therefore the less abundant proteins are masked by more abundant proteins. Consequently, the usual sample preparation steps for mass spectrometry (MS) experiments begin with depletion of high abundant proteins using commercially available immunoaffinity depletion columns (Agilent, Sigma, and Beckman-Coulter). After depletion, fractionation is performed by means of size exclusion chromatography, ion exchange chromatography, and/or isoelectric focusing. However, removal of abundant native high molecular weight proteins can significantly reduce the yield of candidate biomarkers because it has been recently shown that the vast majority oflow abundance biomarkers are non-covalently and endogenously associated with the carrier proteins that are being removed (Lopez et al., Clinical chemistry 2007, 53, (6), 1067-74; Conrads et al., BioTechniques 2006, 40, (6), 799-805; Lowenthal et al., Clin Chem 2005, 51, (10), 1933-45; Lopez et al., Clinical chemistry 2005, 51, (10), 1946-54). Methods, such as size exclusion ultrafiltration under denaturing conditions (Zolotarjova et al., Proteomics 2005, 5, (13), 3304-13), continuous elution denaturing electrophoresis (Camerini et al., Proteomics Clin. Appl. 2007, 1, 176-184), or fractionation of serum by means of nanoporous substrates (Geho et al., Bioconjug Chem 2006, 17, (3), 654-61) have been proposed to solve this problem. Moreover, these same recent findings point to the low molecular weight region of the proteome, as a rich and untapped source of biomarker candidates (Tirumalai et al., Molecular & cellular proteomics 2003, 2, (10), 1096-103; Merrell et al., J of biomolecular techniques 2004, 15, (4), 238-48; Orvisky et al., Proteomics 2006, 6, (9), 2895-902).

In addition to the difficulties associated with the harvest and enrichment of candidate biomarkers from complex natural protein mixtures (such as blood), the stability of these potential biomarkers poses a challenge. Immediately following blood procurement (e.g. by venipuncture) proteins in the serum become susceptible to degradation by endogenous proteases or exogenous environmental proteases, such as proteases associated with the blood clotting process, enzymes shed from blood cells, or associated with bacterial contaminants. Therefore, candidate diagnostic biomarkers in the blood may be subjected to degradation during transportation and storage. This becomes an even more important issue for the fidelity of biomarkers within large repositories of serum and body fluids that are collected from a variety of institutions and locations where samples may be shipped without freezing.

As such, there is a need in the art for particles that allow enrichment and encapsulation of selected classes of proteins and peptides from complex mixtures of biomolecules such as plasma, and protect them from degradation during subsequent sample handling. The captured analytes could then be readily extracted from the particles by electrophoresis allowing for subsequent quantitative analysis. Particles of this type would provide a powerful tool that is uniquely suited for the discovery of novel biomarkers for early stage diseases such as cancer.

Use of harvesting nanoparticles as created in a laboratory by the inventors of the present invention also has been shown to capture, protect from degradation, and amplifY the concentration of low abundance biomarkers in the urine. Human growth hormone within urine at low undetectable concentrations was concentrated by particle sequestration to be readily measured by a standard clinical grade immunoassay. For the first time this labile and low abundance biomarker can now be routinely screened in the urine. Physiologic salt and urea concentration does not affect the function of the particle sequestration. The captured biomarker is preserved and stable at room temperature or at 37C. This finding is applicable to any desired biomarker that can be captured by the particles and uniquely solves a need.

SUMMARY OF THE INVENTION

It is an object of the present invention to provide capture particles for biomarker harvesting. The capture particles are made up of materials that allow for the sequestering of biomarkers to extract them from mixtures and to protect them from degradation. In one embodiment of the present invention, the capture particles have the ability to specifically capture molecular species having a defined molecular size, mass, and or affinity characteristic and are used to isolate molecules of interest from a sample typically containing a plurality of different molecular species. The capture particles are added to the sample and then utilized to capture the molecular species of interest.

It is a further object of the present invention to provide smart hydrogel particles for biomarker harvesting. The smart hydrogel particles of the present invention may have a porosity and overall size that can be changed by changing the environment surrounding the smart hydrogel particles. The smart hydrogel particles may have a porosity that allows for biomarkers to enter the hydrogel under certain conditions, after which, the conditions surrounding the smart hydrogel particle may change so that the biomarkers are sequestered inside of the smart hydrogel particle.

It is a still further object of the present invention to provide capture particles for biomarker harvesting that have an attractant capable of attracting and interacting with a biomarker. It should be noted that the term attractant is hereinafter synonymous with the term bait and affinity monomer. Also, the term mixture is synonymous with the term solution. In certain embodiments, the attractant will be present inside of the capture particle. In other embodiments, the attractant is part of the material that makes up the capture particle itself.

It is a further object of the present invention to provide capture particles for biomarker harvesting having one or more of the following characteristics: a) an ability to select the size and/or mass of the molecule to be captured, b) an ability to select the affinity properties of the molecule to be captured, and/or c) an ability to capture and/or release the desired molecule in response to a physical or chemical treatment. It is yet another object of the present invention to provide capture particles for biomarker harvesting that can be easily isolated and separated from mixtures after sequestering of biomarkers is complete. In certain embodiments of the present invention, the capture particles may have characteristics or modifications that allow for them to be separated from mixtures through the application of physical force, electric or magnetic fields, or by the attraction of a moiety on the particle to target.

It is yet another object of the present invention to provide kits for identifying an analyte present in a mixture or solution. The kits of the present invention have some type of collecting device which is typically filled or coated with the capture particles. A solution or other mixture containing the analyte can then be applied to the collecting device, allowing the capture particles to sequester and isolate the desired analyte for analysis.

It is yet another object of the present invention to provide a micro fluidics system for analysis of analytes captured from a solution. The micro fluidic system will have capture particles of the present invention. The sample containing the analyte to be analyzed is introduced into the micro fluidics system, where the capture particles sequester the analyte. The capture particles are then transferred to a separate location where the analyte is released and analyzed using methods known in the art.

The peptidome/metabolome, populated by small circulating proteins, nucleic acids or metabolites, represents a valuable source of biomarker information reflecting the biologic state of the organism. [1,2] Measurement of circulating biomarker molecules holds great promise as a means to a) detect early stage disease, [3] b) stratify patients into distinct risk subgroups, and c) monitor progression or response to therapy.[4] The low-molecular weight (LMW) region of the blood proteome, which is a mixture of small intact proteins and fragments of large proteins, is an emerging arena for biomarker research. [5] Tissue derived proteins, that are too large to passively enter the blood stream, can be represented as fragments. This LMW region of the proteome is particularly amenable to biomarker discovery based approaches using current mass spectrometry technology.

Nevertheless, despite the recent progress in proteomics discovery and measurement technologies, identification of clinically useful biomarkers has been painfully slow. While this lack of progress is partly due to the inherent analytical difficulties associated with an extraordinarily complex matrix biospecimen such as blood, there are three fundamental and serious physiologic barriers thwarting biomarker discovery and measurement:

-   -   1. The foremost problem in biomarker measurement is the         extremely low abundance (concentration) of candidate markers in         blood, which exist below the detection limits of mass         spectrometry and conventional immunoassays. Such a low abundance         would be expected for early stage disease, the main target of         diagnosis, since the diseased tissue constitutes a small         proportion of the patient's tissue volume.     -   2. The second major problem for biomarker discovery and         measurement is the overwhelming abundance of resident proteins         such as albumin and immunoglobulins, accounting for 90% of         circulating plasma proteins, which confound and mask the         isolation of rare biomarkers.[6] In fact, the vast majority of         low abundance biomarkers are non-covalently and endogenously         associated with the resident proteins such as albumin which         exist in a billion fold excess compared to the rare biomarker.         [7]     -   3. A third serious challenge for biomarker measurement is the         propensity for the low abundance biomarkers to be rapidly         degraded by endogenous and exogenous proteinases immediately         after the blood sample is drawn from the patient. Degradation of         candidate biomarkers occurs also during transportation and         storage of blood, generating serious false positive and false         negative results. [8]

The field of nanotechnology offers fresh approaches to address these three fundamental physiologic barriers to biomarker discovery. We have engineered smart hydrogel core-shell nanoparticles that will overcome these three barriers to biomarker discovery and measurement, and will do so in one step, in solution. [9]

A hydrogel particle is a cross linked particle of sub-micrometer size made of hydrophilic polymers capable of swelling and contracting as a result of the application of an environmental trigger, e.g., temperature, pH, ionic strength or electric field. [10-14] Hydrogel particles have extensive applications in biomedicine and biotechnology [15-18] because of their high biocompatibility and unique physiochemical properties. Recently we modified hydrogel particles in an attempt to develop a technology that can overcome all of the aforementioned major physiologic challenges for biomarker isolation and measurement. [9] These particles rapidly encapsulate, concentrate, and protect from degradation, low molecular weight and low abundance proteins. Despite the promise of this feasibility study [9] it remained to be proven whether such hydrogel particle technology could be shown to be applicable to a clinically relevant, highly labile, and very low abundance biomarker. To address this challenge we created a new class of core shell particles and tailored the core bait to specifically capture a model biomarker Platelet Derived Growth Factor (PDGF). We then used three independent experimental systems to test whether the new particles could accomplish the following a) Rapidly harvest all of the solution phase PDGF molecules within a complex mixture of high abundance proteins including whole serum, b) Concentrate the captured PDGF into a small volume that was a small fraction of the starting volume, while completely excluding high abundance proteins such as albumin. This concentration step has the potential to magnify the detectable level of the marker in a small volume that is required for input into a measurement system such as an immunoassay platform or mass spectrometry. And c) Protect the captured PDGF from degradation by exogenous degradative enzymes introduced at high concentration. The three independent experimental approaches employed for the present study were 1) A clinical grade ELISA immunoassay, 2) Gel Electrophoresis of the starting solution, the supernatant and the particle contents followed by western blotting, and 3) Mass Spectrometry analysis of the starting solution compared to the particle capture eluate.

-   -   4. Core-shell hydrogel particles are of particular interest         because the properties of the core and shell can be tailored         separately to suit a particular application. In many core-shell         particle systems used for drug delivery, the core is designed to         have the properties required for its intended application. [12,         19-21] The shell is then separately added to surround and shield         the core. The thickness of the shell can be modified to alter         permeability or porosity.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. Chemical composition of particles. Structure of (A) Nisopropylacrylamide (NIPAm) and its polymer, (B) methylenebisacrylamide and (C) NIP Am and acrylic acid and their polymers.

FIG. 2. Particle characterization. (A) Light scattering measurement of NIP Am particle size as a function of temperature (diameter decreases as temperature increases). (B) Plots of correlation of the size of NIPAmJAAc particles with temperature (diameter decreases as temperature increases) and pH (diameter decreases as pH decreases). AFM images of (C) NIPAm particles and (D) NIPAmJ AAc particles on mica.

FIG. 3. Schematic drawing of molecular sieving of particles in solution. Low molecular weight proteins are harvested; high molecular weight proteins are excluded.

FIG. 4. Flow cytometry analyses of FITC-incubated particles. (A) Uptake is dose dependent. (B) Uptake rapidly reaches saturation with a FITC concentration of 20).IM. NIP Am particles were also incubated with FITC-labeled bovine serum albumin (BSA), MW 66,000 Da, with a dye:molecule ratio of 1:1 (FITC-BSA, Sigma), FITC labeled insulin MW 3,500 Da, with a dye:molecule ratio of 1:7 (Invitrogen), or FITC labeled myoglobin MW 17,000 Da, with a dye:molecule ratio of 1.36. Myoglobin (Sigma) was FITC labeled by means of the HOOK-Dye Labeling Kit (G Bioscience) in accordance of the vendor's instructions. Concentrations of all fluorescent species were adjusted in order to equalize the fluorescence signal.

FIG. 5. NIPAm particles incubated with FITC and FITC-labeled proteins: Flow cytometry measurements of (A) BSA and insulin, (B) myoglobin and free FITe. (C) SDS-PAGE of particles incubated with insulin: Lane 1) insulin solution (Control), 2) NIPAm supernatant (Out, substance excluded from the particles), 3) wash 1,4) wash 2, 5) NIPAm particles (In, substance captured by the particles). (D) SDS-PAGE of NIP Am particles incubated with BSA and myoglobin: 1) BSA and myoglobin (Control), 2) NIPAm supernatant (Out), 3) wash 2, 4) NIPAm particles (In). BSA is totally excluded.

FIG. 6. Schematic depiction of affinity-based sequestering.

FIG. 7. Protein sequestering by NIPAmI AAc particles (+bait) versus NIP Am particles (−bait), SDS-PAGE analysis of (A) Myoglobin (aqueous solution, pH 5.5) sequestration by particles + and −bait. Lane 1) myoglobin, 2) NIPAm supernatant (Out), 3) NIPAm particle (In), 4) NIPAmIAAc supernatant (Out), 5) NIPAmIAAc particle (In), 6) NIP Ami AAc particles 1:64, 7) NIP Ami AAc particles 1:32, 8) NIP Ami AAc particles 1:128, and 9) NIPAmIAAc particles 1:256. (B) BSA and myoglobin sequestration by particles+bait (NIPAmIAAc) at two pH values. Lane 1) BSA and myoglobin, pH 5.5, 2) NIPAmIAAc supernatant (Out) pH 5.5, 3) wash 3 pH 5.5, 4) NIPAmIAAc particles (In) pH 5.5, 5) wash 2 pH 5.5, 6) wash 1 pH 5.5, 7) BSA and myoglobin, pH 8, 8) NIPAmIAAc supernatant (Out) pH 8, and 9) NIPAmIAAc particles (In) pH 8.

FIG. 8. (A) SDS-PAGE analysis of particles − and +bait incubated with BSA and lysozyme: Lane 1) BSA and lysozyme solution prior to particle introduction, 2) NIP Am (−bait) supernatant (Out), 3) wash 3, 4) NIPAm (−bait) particles (In), 5) wash 2,6) wash 1,7) NIPAmIAAc (+bait) supernatant (Out), 8) wash 3, and 9) NIPAmIAAc (+bait) particles (In). (B) SDS-PAGE analysis of NIPAmIAAc particles (+bait) incubated with molecular weight (MW) markers: 1) MW markers, 2) NIPAmIAAc supernatant (Out), and 3) NIPAmIAAc particles (In).

FIG. 9. SDS PAGE analysis of particles+bait incubated with PDGF Band BSA. Lane 1) BSA and PDGF B, 2) NIPAmIAAc supernatant (Out), 3) NIPAmIAAc particles (In).

FIG. 10. Flow cytometry analysis of (A) NIPAm and (B) NIPAmIAAc particles incubated with FITe-labeled insulin aqueous solution and FITe-labeled insulin spiked in serum, respectively.

FIG. 11. Flow cytometry time course studies of (A) NIP Am and (B) NIP Ami AAc particles incubated with FITe-labeled insulin.

FIG. 12. Uptake time course study (A) Mean values of the percentage, relative to the initial amount, of lysozyme in solution incubated with two quantities of NIPAmIAAc particles as measured by RPPAs (three replicate analyses and standard deviation shown). (B) SDS-PAGE analysis of a lysozyme and BSA solution incubated with NIP Ami AAc particles. Lane 1) BSA and lysozyme solution. 2-11) alternating supernatant (Out) and particles (In) for each of 5, 10, 20, 30, and 60 minutes incubation times. Lysozyme uptake is rapid and complete, while BSA exclusion is total.

FIG. 13. Schematic drawing illustrating the ability of particles to protect proteins from enzymatic degradation.

FIG. 14. NIPAmIAAc particles (+bait) protect bound proteins from degradation by enzymes that may be present. (A) NIPAmIAAc particles incubated with a solution containing lysozyme and trypsin for 1 hr: Lane 1) lysozyme, 2) lysozyme incubated with trypsin, 3) NIPAmIAAc supernatant (Out), 4) NIPAmIAAc particles (In), 5) BSA and lysozyme, 6) BSA and lysozyme+protease, 7) NIPAmIAAc particles supernatant (Out), and 8) NIPAmIAAc particles (In). (B) NIPAmIAAc particles incubated overnight with BSA, lysozyme, and trypsin: Lane 1) lysozyme, 2) trypsin, 3) lysozyme+trypsin, 4) NIPAmIAAc supernatant (Out), 5) NIPAmIAAC particles (In), 6) lysozyme and BSA, 7) BSA and lysozyme+protease, 8) NIPAmIAAc supernatant (Out), and 9) NIPAmIAAc particles (In).

FIG. 15. SDS PAGE analysis of reduced and alkylated lysozyme exposed to tryptic digestion and incubated with particles+bait and −bait. (A) Reduced and alkylated lysozyme+trypsin incubated with NIPAmIAAc particles: Lane 1) lysozyme, 2) reduced and alkylated lysozyme, 3) +trypsin, 4) NIPAmIAAc supernatant (Out), 5) NIPAmIAAc particles (In). (B) Reduced and alkylated lysozyme incubated with NIPAm particles: lane 1) NIPAm particles supernatant (Out), 2) NIPAm particles (In), 3) +trypsin NIP Am supernatant (Out), 4)+trypsin NIPAm particles (In), 5) +trypsin, 6) BSA+reduced and alkylated protein solution incubated with NIP Am particles, supernatant (Out), 7) NIPAm particles (In).

FIG. 16. Core shell particles have the same molecular weight sieving as NIP Ami AAc particles. Control protein solution was incubated with NIP Ami AAc and core shell particles. Lane 1) control protein solution, 2) NIPAmI AAc particles supernatant (Out), 3) NIPAmIAAc particles (In), 4) core shell particles supernatant (Out), 5) core shell particles (In).

FIG. 17. Core shell particles protect lysozyme form chymotrypsin proteolysis. Lane 1) lysozyme, 2) chymotrypsin, 3) lysozyme+chymotrypsin, 4) lysozyme+chymotrypsin incubated with core shell particles, supernatant (Out), 5) lysozyme+chymotrypsin incubated with core shell particles, particles (In), 6) lysozyme+BSA+chymotrypsin, 7) lysozyme+BSA+chymotrypsin incubated with core shell particles, supernatant, 8) lysozyme+BSA+chymotrypsin incubated with core shell particles, particles (In), 9) lysozyme+BSA.

FIG. 18. Light scattering characterization was conducted on particles during the synthesis process and at the end of the process in order to compare the sizes of the core and the core shell particles.

FIG. 19. The particles were retained in the stacking region of the gel while all of the captured proteins were electroeluted from particles and resolved in the gel. There was no detectable association of BSA with the particles, and the particles completely sequestered all the solution phase PDGF while completely excluding the BSA.

FIG. 20. Proteins were eluted from the washed particles by means of two subsequent elution steps with 60% acetonitrile and 2% acetic acid.

FIG. 21. Trypsin action on PDGF in the absence of particles was evident after 10 minutes and almost complete after one hour, as indicated by nearly undetectable PDGF bands at 14,000-17,000 Da (Lanes 6-8).

FIG. 22. Particles excluded the high molecular weight proteins which remained in the supernatant (Lane 2 and Lane 5) and at the same time they concentrated PDGF (Lane 3 and Lane 6) that was spiked in serum at two different concentrations.

FIG. 23. PDGF+BSA and Trypsin is shown.

FIG. 24. Serum+PDGF is shown.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides capture particles for harvesting biomarkers as wells as methods for using those particles. The capture particles of the present invention are capable of selectively selecting specific biomarkers from a mixture, after which the capture particles are removed from the mixture and the biomarkers are released from the capture particles.

In certain embodiments of the invention, the capture particles have one or more of the following characteristics: a) an ability to select the size and/or mass of the molecule to be captured, b) an ability to select the affinity properties of the molecule to be captured, and/or c) an ability to capture and/or release the desired molecule in response to a physical or chemical treatment. The particles of the present invention may accomplish this task in microvolumes, eliminating the need for the conventional multi-step procedures requiring, e.g., affinity columns, reverse phase columns and molecular sieve steps. The characteristics of the capture particles depend on the materials used to construct the capture particles. Examples of certain types of capture particles made from certain materials are set forth herein, however, it will be obvious to one of skill in the art that there are other combinations and variations of capture particles not explicitly set forth in this specification that have characteristics which can be determined from the way they are constructed and which fall within the scope of the claims set forth below.

Throughout this description, the harvesting of biomarkers or other analytes will be described. The capture particles and methods of the present invention can be adapted to harvest any type of molecule or compound of interest, both biomarkers produced by a living source or other analytes. It certain embodiments of the invention, the analyte to be harvested may be a metabolite, protein, RNA, micro RNA, DNA glycoprotein, lipid, glycolipid, proteolipid, hormone, cytokine, growth factor, biomarker, drug compound, synthetic organic compound, volatile odorant, toxicant or pollutant. It should be apparent to one of skill in the art that the present invention is not limited in any way to the harvesting of specific types of molecules and that molecules from any source present in any type of mixture may be harvested using the compositions and methods of the invention.

In certain embodiments, the capture particles of the present invention can be comprised of a molecular sieve material. By this, it is meant that the material is porous, lattice-like, honeycombed, or has other properties that permit analytes of a defined molecular mass or weight to enter. The size of the sieve pore is a determinant of whether the analyte can penetrate the capture particle. The particle, itself, can be of any suitable size, e.g., 1 nm or less; from about 1 nm-100).Im; from about 5 nm-50).Im; from about 10 nm-20).Im; from about 10 nm-10).Im; including any and all values in between. The particles of the present invention may have any suitable shape, including, but not limited to, spheres, tubes, branched structures, polyhedrons and micro-fluidic valves.

The sieve materials used in constructing the capture particles of the present invention may be designed so as to allow only analytes of a certain size to enter the capture particles. The size cutoff of the capture particles will be dependent on the manner in which the particles are to be used. The cutoff size, as used herein, is meant to describe the approximate size of an analyte which is able to enter the capture particle. For example, molecular weight (MW) cutoff size of 50 kDa means that molecules of approximately 50 kDa or less in size will be able to enter the capture particles, while molecules of approximately more than 50 KDa will be excluded from the particles. In certain embodiments, the particles may have a MW cutoff size of from about 5 kDa to about 100 kDa, although particles having other MW cutoff sizes outside of this range are also contemplated. As described herein, the capture particles of the present invention may be made of “smart” materials capable of changing size in response to stimuli. In such cases, the MW cutoff size of the particle may change as the size of the particles changes, e.g. a particle may have a specific MW cutoff size under certain condition's and a different MW cutoff size under other conditions.

A feature of the capture particles of the present invention is their ability to “trap” or sequester an analyte once it has entered the particle. Trapping is achieved by using sieve materials which are capable of contracting and/or expanding in response to a physical or chemical treatment for making the particles. For example, materials can be utilized which, when subjected to a chemical or physical treatment, contract or shrink, thereby trapping the analyte inside. Such materials may be referred to as “smart materials” which have the ability to change shape or size by subject to a physical or chemical treatment.

Any material having these properties can be utilized without restriction to make the capture particles of the present invention. In certain embodiments, these materials are polymers made of: acrylamide and derivatives thereof, N-isopropylacrylamide (e.g., Jones and Lyon, Macromolecules, 36:1988-1993, 2003; Jones and Lyon, Macromolecules, 33:8310-8306, 2000) and other N-alkyl substituted acrylamides; N,N methylenebisacrylamide, N,N-cystaminebisacrylamide, N-vinylalkylamides, acrylic acid, methacrylic acid, allylamine, styrene, benzyl glutamate, 2-ethylacrylic acid, 4-vinylpyridine, silicone, hydroxyethyl methacrylate, ethylene oxide, butylenes terephthalate, 2-acrylamido-2-methyl-1-propanesulfonic acid, vinylpyrrolidone, and ethylene-vinyl acetate. In other embodiments of the present invention, the capture particles may be made of biodegradable polymers made up of lactide, glycolide, caprolactone, and hydroxyalkanoate. In still other embodiments of the present invention, the polymers may be made up of chitosan, hyaluronic acid, starch, cellulose and agarose. The polymers used to make the capture particles of the present invention mayor may not be made up of crosslinkable units. In the case of crosslinkable polymers, the crosslinks may be formed either permanently or reversibly. The polymers contemplated by the present invention may be polymers having a single repeating unit or may be co-polymers having two or more monomer units which are included in the polymer.

Other examples of materials used may be ferroelectric liquid crystalline elastomers; piezoelectric polymers; “smart” hydro gels, gels, ceramics, alloys, and polymers, etc. Other examples of suitable materials may be found in Galaev et al., Pages 835-849; Zentel; Pages 850-860; Harrison and Ounaies, Pages 860-873; in Encyclopedia of Small Materials, Volumes 1-2, Edited by, Schwartz, Mel© 2002 John Wiley & Sons. Examples of other materials suitable as slevmg materials are woven or cross-linked nanOWIres, carbon nanotubes, metal colloids, clatherins, collagen, modified polysaccharides, silicon, silica, linked peptides comprised of amino acids, polymers composed of nucleic acids (see, e.g. Chittimalla et al., J Am. Chem. Soc., 2005, 127 (32), 11436-41), amino acid polymers, lipids (see, e.g. Advanced Drug Delivery Reviews, Lipid Nanoparticles: Recent Advances, 2007, 59 (6), 375-530), self-assembled viruses, and self-assembled proteins. The capture particles can be prepared routinely by methods known in the art or as described in any of the above-mentioned references.

Physical and/or chemical treatments that may be utilized to contract and/or expand the sieve material include thermal, electrical, magnetic, ultrasound, pressure, radiant, laser, osmotic, pH, salt, enzymatic, oxidation/reduction, dehydration/rehydration, ultraviolet, radiation, high intensity red light, and similar treatments as are known in the art.

The sieve material can reversibly or non-reversibly contract or shrink. For example, the capture particles can be placed in a mixture where the analytes are permitted to penetrate, and then non-reversibly shrunk to capture the analyte. This could be useful where the objective is to remove a contaminant from a solution, and it is not necessary to analyze or further evaluate the nature of the captured analyte, thus not requiring it to be expanded. Alternatively, non-reversible capture particles can be broken apart by sonication or other disruptive forces which destroy the integrity of the particle.

The capture particles can further comprise an attractant capable of attracting and interacting with a biomarker. The attractants of the present invention may be any substance which is capable of specifically interacting with an analyte of interest. In certain embodiments, the attractant is an affinity ligand and may be: antibodies and derivatives thereof (e.g., Fab fragments and single-chain antibodies); binding proteins and peptides (e.g., receptors or fragments thereof for specific ligands and polyhistidine peptides), including modified proteins; binding pairs (such as streptavidin/biotin); substrates; metals; chelating agents; nucleic acids; aptamers; enzyme-binding pockets; lectins; calixarenes for the uptake of small molecules; metals or metal salts (e.g. Fe for heme groups, Ti02 for phosphorylated peptides and proteins); affinity dyes; pharmaceutically active compounds; peptides and fullerenes, lipophilic compounds, aromatic compounds and/or an affinity group that is specific for an analyte of interest. The capture particles may also be formed using molecular imprinting techniques, as are well known in the art. In these embodiments of the present invention, the capture particles may be imprinted to bind specific molecules or families of molecules

In certain other embodiments of the invention, the attractant may be a chemical moiety capable of interacting chemically or electrostatically with the analyte. In these embodiments of the invention, the attractant may include a carboxyl group, amine group, lipid, phosphate group, amide group, hydroxyl group, ester group, acrylic group, thiol group, acrylic acid, hydrophobic surface, hydrophilic surface or any other moiety capable of interacting chemically or electrostatically with the analyte.

The attractants can be associated with the capture particle in any suitable way. For example, they can be used as a nucleus or core around which the sieve material is overlayed or deposited/nucleated in order to form the capture particle; they can be directly incorporated into the sieve material prior to forming the particle (i.e. where the attractant is a component of the sieve material); they can be conventionally coupled (covalently or noncovalently) to the pore surfaces of the sieve material; etc. The attractants can also be loaded into the capture particle by expanding the sieve material through appropriate physical or chemical treatment to reach a porosity that is large enough to admit the ligand, and then contacting the sieve material with the attractant under conditions effective for it to enter the particle. Once the particle is loaded with the attractant, it can be shrunk by appropriate physical or chemical treatment, thereby reducing the sieve material's porosity, such that target analytes are still able to penetrate the particle, but larger analytes are excluded. The sieve porosity can be reduced after the attractant loading step to pore size which is small enough to block the affinity ligand from diffusing out, making it unnecessary to link the attractant to the sieve material. However, if desired, coupling processes can be used to link the attractant to the sieve material.

Capture particles baited with affinity ligands provide an analyte selection step, in addition to selection for analyte size or mass. For example, a capture particle can be expanded to allow analytes to penetrate into it, and then the analytes can be further selected by their ability to specifically bind to an affinity ligand associated with the capture particle. After the binding step is achieved (e.g., after equilibrium is reached), the particles can be separated and subjected to washing steps to remove unbound non-target analytes, and then optionally shrunk by a chemical or physical treatment.

In certain embodiments of the invention, the attractant is a component of a sieve material. For example, the sieve material may be a co-polymer having monomeric units that have an electrostatic charge. In certain embodiments, the co-polymer is made up of uncharged structural monomer units and affinity monomer units, so that the sieve material itself is capable of attracting an analyte to be captured. In certain embodiments, the affinity monomer units may be positively or negatively charged so that the sieve material has an overall electrostatic charge. In these embodiments, is also contemplated that the charged monomeric units may be such so that their charge can be changed by changing the environment of the sieve material, e.g. changing the pH or temperature of the media surrounding the capture particles. In these embodiments, the capture particles provide both size and affinity selection of analytes.

In certain embodiments where the sieve material is a charged co-polymer, the charged monomeric units may have moieties that allow them to be charged under certain conditions. For example, negatively charged monomers may have carboxylic acid groups, hydroxyl groups, thiol groups, phosphate groups or other groups capable of carrying a negative charge. In certain embodiments of the invention, the negatively charged monomer is acrylic acid or another monomer with a carboxylic acid group. Positively charged monomers may have amine, amide groups or other groups capable of carrying a positive charge. In certain embodiments of the invention, the positively charged monomers are allylamine or chitosan.

In other embodiments of the invention where the sieve material is a co-polymer, affinity monomer units may be integrated into the sieve material that allow for attraction of various type of analytes. For example, co-polymers may be integrated with monomers having: affinity dyes having affinity for proteins and peptides; boronic acid groups having affinity for carbohydrates, nucleic acids and glycopeptides or glycoproteins; cyclodextrins having affinity for small molecules; calixarenes having affinity for small molecules; porphyrin groups having affinity for metal ions; and aliphatic groups having affinity for lipids.

In certain embodiments of the present invention the sieve material is an Nisoproylacrylamide (NIP Am), acrylic acid (Mc) copolymer whose pendant carboxylic acid (C02H) groups are functionalized with a wide range of amino or alcohol terminated molecules. These molecules can include alkanes, other greasy moieties to capture the lipid content of the solution, or dyes. In certain other embodiments of the present invention, the particles have a core made of a NIP Am AAc co-polymer that is surrounded by a shell polymer layer made up of only NIP Am.

The capture particles may also further comprise detectable labels. Detectable labels may be any moiety or substance that can be detected by any means. These include quantum dots, fluorescent labels, enzymes, magnetic particles, etc. The detectable label can be associated with any region of the capture particle, including its pores and exterior surface.

Detectable labels are useful in a number of ways, including for sorting different classes of capture particles. For example, different classes of capture particles can be produced, where each class possesses a different characteristic (e.g., a different pore size and/or a different attractant), and each carries a different detectable label associated with each class of particles. This enables the property of the particle class (e.g., able to bind to a specific attractant) to be identified by determining which detectable label it bears. For instance, a particle with a single chain antibody for PSA can be labeled with FITC, and a particle containing an antibody for a-Methylacyl-CoA racemase (AMACR) can be labeled with TRITC. After performing the entrapment step, the particles can be sorted by flow cytometry using fluorescent-activated cell sorting, separating the PSA-containing particles from the AMACR-containing particles. In other embodiments, the capture particles can be functionalized with lipophilic carbocyanine dyes and then their lipid content can be separated using thin layer chromatography.

Capture particles can be moved in solution or other media by the application of electrical fields, magnetic fields, through the use of laser tweezers, or by their affinity with solvent. If the capture particles have an overall electric charge, they may be moved by application of an electric field. This may be especially applicable when the sieve material has been modified so as to have an electrostatic charge. For example, an electric field can be applied across a medium containing negatively charged capture particles, and the capture particles would move towards the positive electrode of the device applying the electrical field.

The capture particles may also be modified to have magnetic moieties that are attracted to a magnet. In certain embodiments of the present invention, this may be done by forming the sieve material around a magnetic core, such as a Fe304 core. In other embodiments, the surface of the capture particles may be fully or partially coated with magnetic nanoparticles (see, e.g. Wong et al., J Magnetism and Magnetic Materials, 2007, 311 (1), 219-23). It is further contemplated that co-polymers may be formed having magnetic elements directly incorporated into the polymers.

It is also contemplated that the capture particles may be modified to have surface markers that can be easily bound by specific targets, e.g. the particles may have biotin, glutathione-S-transferase or 6-histidine tags that can be bound by streptavidin, glutathione, and nickel substrates respectively. The particles can also be formed using reversible crosslinkers such as those formed from disulfide bonds that can be reversed by DTT. In these embodiments of the invention, a solution containing capture particles may be mixed with beads having a suitable substrate, for example, biotin labeled particles may be mixed with streptavidin labeled beads. After being allowed to bind to one another, the beads could be removed from the solution using centrifugation or other techniques known in the art, bringing the capture particles with them.

Certain embodiments of the invention relate to solution-phase capture particles and methods of using them to isolate analytes from a sample having one or more of the following steps, e.g., contacting a sample comprising analytes with solution-phase capture particles under conditions effective for the capture particles to reversibly and selectively trap analytes of a defined molecular mass or particle size, where the capture particles are made with a molecular sieve material which is capable of reversibly trapping and releasing an analyte of a defined particle size or molecular mass.

The capture particles of the present invention may allow for the protection of analytes from degradation by proteases and other factors. The capture particles may do this by excluding the proteases from the particle by the size cut-off and/or the affinity characteristics of the particle. The capture particles may also prevent proteases from degrading analytes because the analytes and proteases are so tightly bound as to prevent the steric alignment necessary for the protease to cleave the analyte. In these cases, even though the protease is capable of entering the capture particle, the analyte remains intact.

The capture particles of the present invention may also be used for concentrating low abundance analytes from a fluid. If an analyte is present in a fluid at a low concentration, the capture particles of the present invention may be used to harvest the analyte from the original fluid. After the analyte is harvested, it may then be released into a second fluid having a smaller volume. In this way, analytes having concentrations below the limits of detection of various analytical methods in their original fluids may be concentrated so that they have a concentration that can easily be detected and analyzed.

In certain embodiments of the present invention, the capture particles described may be part of kits which may be used for isolating and/or identifying an analyte. The kits may have any type of collection device for collecting the solution or other type of mixture containing the analyte. In some embodiments, the collection device is a container, such as a vacu-tainer, tube, cartridge or micro fluidic device. It is contemplated that the capture particles may be present in the container, or, alternatively, a layer of capture particles may be formed on the container. In other embodiments, the collecting devices are sheets of fabric or polymeric material capable of containing a layer of capture particles. In these embodiments, the capture particle may be formed into a type of patch, which may be applied to a surface from which an analyte of interest is to be isolated or over which an analyte of interest passes. In one embodiment, the patch may be a patch that can be applied to the skin, allowing analytes to be isolated from the surface of the skin.

Also contemplated by the present invention is a system where particles can be continuously moved among different steps. In general:

Step 1: Capture particles are mixed with a sample comprising analytes;

Step 2: Capture particles are separated from solution phase moieties that have not been captured; and

Step 3: Analytes are eluted from particles and analyzed.

In these embodiments of the invention, the system is fully self-contained and automated so that a sample is introduced into the system and a result is obtained without requiring any other user manipulation. Such a system may be contained in a micro fluidic system or may be a larger, bench-top type system.

In general, a sample is added to a chamber containing capture particles and the analyte of interest is sequestered. The environmental conditions of the chamber may then be changed so that the capture particles are reduced in size as described herein, trapping the analytes inside. The capture particles can then be moved to a new chamber using the methods described herein, separating the analytes from the remainder of the sample.

Analysis can then be done using methods known in the art, including mass spectrometry, nuclear magnetic resonance, infrared spectroscopy, solid phase immunoassay (e.g. ELISA and the like) immunoprecipitation, colorometric assay, radiometric assay, fluorescent assay, flow bead/flow cytometry, western blotting, protein sequencing and any chemistry analytic method for analysis of metabolites, drugs, small molecules or proteins.

Beyond the solution phase capture process, the particles can also be used to coat support surfaces, to impregnate layers and to fill slabs. Other examples include coating a patch with particles held by a mesh, and applying the patch to a patient's skin to capture analytes present on and in the skin.

Any sample can be utilized without restriction, including biological fluids, such as blood, blood components, cerebral spinal fluid, lymph, cellysates, tissue lysates, stool, urine, lymph, ascites, semen, etc.; environment samples, such as soil samples or extracts, ocean, pond, or river waters; water tower and drinking water samples; samples from chemical synthetic reactions; food samples; etc. For example, the methods discussed herein can be used to detect contaminants in food, drinking water, and environment samples. Any molecule of interest may be harvested using the present invention, including, organic molecules, inorganic molecules, polypeptides, carbohydrates, nucleic acids, lipids, drugs, antibodies, ligands, lipoproteins. glycoproteins, fatty acids, glycans, derivatives thereof, and combinations thereof. Analytes include biomolecules which are shed from cell surfaces, released from cells (e.g., by exocytosis, lysis, etc.), metabolites, degradation products, protease digestion products, and the like, without limitation. In certain embodiments of the invention, the methods can be utilized to entrap molecules in a biological fluid of a low molecular weight, especially those that would be excluded from the body by normal glomerular (kidney) filtration (e.g., molecules less that 30,000 Daltons) which are soluble and free-floating in the fluid or which are associated with carrier proteins. In general, the present invention can be used to capture any analyte of interest whose detection is desired. The particles can be used in solution during any chemical reaction to selectively capture reaction products and therefore lower products concentration in solution. This can enable the chemical reaction to go to completion or to drive the chemical reaction to completion by sequestering one or more reaction species as they accumulate over time. With respect to body fluids, the capture particles of the present invention can also be used to detect exogenous molecules, i.e., is a molecule that was introduced into the body of the subject from whom the sample was obtained. Exogenous molecules can be actively or passively introduced into the subject. Examples of exogenous molecules include molecules present in, or in the form of, drugs, foods, tobacco, environmental products and contaminants (e.g., pesticides, carbon monoxide, etc), and essentially any molecule that enters the subject body through any route. Exogenous molecules also include their metabolites, by-products, and degradation products as processed or transformed in the body. The particles can also be used as a tool to clear toxins from the blood. The particles can be applied for dialysis of blood by clearing urea or to eliminate cholesterol in excess to prevent heart attacks.

It is also contemplated that different populations of capture particles can be used at the same time, each having different characteristics with respect to the molecule species they are able to capture. The different populations can be univocally tagged, e.g. with fluorescent dyes, and can afterwards be separated, e.g. with flow cytometry. This strategy enables a total extraction and separation of multiple species to be performed in a single step.

Further Embodiments of the Present Invention

Nanoparticle Technology for Biomarker Enrichment and Preservation

In order to directly address the challenges of low abundance and preservation, in certain embodiments, this invention aims to create and evaluate “smart” nanoparticles that harvest (accumulate) selected classes of proteins in solution when added to complex mixtures of proteins such as plasma. The deliverable technology will be novel porous harvesting particles that have a unique structure capable of sorting molecules in solution based on both size and/or affinity. Moreover, the porosity of the particles may be thermally modifiable such that captured analyte (e.g. proteins) can later be released for analysis. In addition, the proteins or chemical entities captured within the particles may be protected from degradation by enzymes or microbial growth.

This proposed technology can address the need for a means to enrich, isolate, and preserve low-abundance proteins and peptides in blood, urine and tissues. Such low abundance molecules are expected to contain the most specific information about the state of a small disease lesion. In one embodiment the proposed technology consists of smart nanoparticles that can be pre-dispensed into a collection tube. Once the nanoparticles are suspended within the body fluid, or tissue lysate for example, the particles automatically (in one step) perform affinity chromatography and/or size exclusion chromatography in solution. The proteins and other metabolites (candidate biomarkers) captured within the smart particles can be therefore bonded and/or sequestered and protected from substantial degradation. By tuning the pore size and affinity properties of the smart particle populations, highly specific subsets of biomarkers can be captured and enriched from the entire volume of the procured fluid. This will enable room-temperature preservation and enrichment of low-molecular weight proteomic biomarkers. Following transport of the collection tube to the analysis lab, the nanoparticles can be easily isolated, so that the bound/sequestered biomarker cargo can be released for characterization using any analytical technique. In an alternative method, the biomarkers may be accessed via destructive treatment of the nanoparticles.

This technology can be of low cost and applicable in the routine clinical setting for seamless collection and immediate preservation of blood biomarkers. This transcends the large research hospital environment and extends most acutely to the private practice, where most patients receive therapy. The fabrication of large quantities of uniform “smart” one-micron-sized nanoparticles is certainly feasible, while other sizes larger or smaller are also possible and equally applicable. As described below, the particles can capture, accumulate, and purify labeled subsets of molecules from complex mixtures of molecules, such as serum.

Rationale for Choosing Smart Particles for Biomarker Harvesting

Thermoresponsive polymer gels are commonly referred to as ‘smart gels’ and display a controllable, nonlinear response to changes in local solution temperature, pH or external energy application (Saunders, et al., 1999 Advances in Colloid and Interface Science 80, 1; Pelton, 2000, Advances in Colloid and interface Science 85, 1). Such polymers are comprised of crosslinked chains that undergo a thermodynamically favored phase separation leading to a change in gel volume (Tanaka, et al., 1979, Phys. Rev. Lett. 42, 1556; Tanaka, et al., 1978, Phys. Rev. Lett. 40,820). The gels can be synthesized in bulk to take on the shape of the container or may be synthesized into particles ranging in diameter from 4 nm-100 μm (Tanaka, et al., 1980, Phys. Rev. Lett. 45, 1636; Tanaka, et al., 1985, Phys. Rev. Lett. 55, 2455). In each case, the internal structure of the material is composed of flexible chains creating a soft, porous structure that can reversibly expand or contract according to the local conditions of the solution. An example of a “smart” polymer is poly(N-isopropylacrylamide) (pNIPAm), which has a lower critical solution temperature (LCST) of 31° C. in water (Jones, 2003, School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Ga., p. 193). Below this temperature, the polymer matrix is swollen with solvent molecules, where hydrogen bonding occurs between the water and amide groups along the polymer backbone (Jones, 2003, School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Ga., p. 193). As the temperature is increased above the LCST, hydrogen bonds are broken and water is excluded from the internal matrix, while hydrophobic interactions begin to dominate between the isopropyl groups, leading to a decrease in overall volume. This technology can be applied to separating biomarkers for identification.

One aspect of the present invention describes a molecular sieve portion of the capture-particles while another aspect pertains to an analyte binding (bait capture) portion. It is feasible to combine bait capture with molecular sieving into a single particle. A common means of fractionating complex mixtures of proteins is to use two classes of sequential chromatographic steps based on affinity and molecular sizing (Adkins, et al., 2002, Mol Cell Proteomics 1, 947). Analysis of a complex and highly concentrated mixture such as plasma usually starts with dilution of the sample and removal of high abundance proteins such as albumin prior to chromatography and gel electrophoresis. The smart particle technology disclosed herein accomplishes both steps of the separation without the use of chromatography or dilution. More specifically, added selectivity is enabled through the addition of bait molecules into the particle that bind/sequester a restricted population of biomarkers. Acrylic acid (Mc), for example, can be integrated into the particle and function as a tunable affinity resin. For example, at low pH (3.5), the Mc within the particle will be predominately protonated, bearing a positive charge at that pH. At higher pH conditions, the Mc moieties will be either partially or predominately deprotonated, which will create an intrinsic, charge based affinity element for positively charged proteins. By integrating Mc into the microgel, both the charge properties and the pore size of the particles provide a means to doubly fractionate proteins from complex mixtures like serum.

Another aspect of the invention deals with preservation by sequestration/binding of analytes therefore allowing one to stabilize analytes (e.g candidate biomarkers) in solution at room temperature. This can accomplished by their sequestration within the porous nanoparticles. It is hypothesized that proteins or molecules sequestered within the nanoparticles will not be available for access by solution phase degradative enzymes. Such enzymes may not be able to penetrate the pores of the particle because of their larger size.

Moreover, the affinity capture and immobilization of the candidate biomarker molecule will hinder the 3-D availability of the biomarker molecule such that the enzyme substrate complex can not functionally form within the particle. This concept is somewhat analogous to the stabilization of proteins by precipitation or precipitation fixation. Applying capillary electrophoresis and mass spectrometry sequencing, we can study the degradation induced by exogenous serine or metalloproteinases, and compare the rate of fragmentation of proteins sequestered in particles versus those free in solution. Starting with defined mixtures of known and pre-characterized, or pre labeled proteins, we can progress to protein capture and stabilization within human serum and plasma reference samples.

Capture-Particles

In certain embodiments, the present invention provides a method and composition for separating and capturing molecular species from samples. In one embodiment of the invention, smart particles which have the ability to specifically capture molecular species having a defined molecular size, mass, and/or affinity characteristic are used to isolate molecules of interest from a sample typically containing a plurality of different molecular species with varying sizes. The particles can be added to the sample and then utilized to capture the molecular species of interest.

The particles can have one or more of the following functionalities: a) an ability to select the size, mass, and/or affinity property of the molecule to be captured, and/or b) an ability to capture and/or release the desired molecule in response to a physical or chemical treatment. The particles can accomplish this task in microvolumes, eliminating the need for the conventional multi-step procedures that utilize affinity columns, reverse phase columns, and other standard purification reagents and devices. Moreover, different classes of capture-particles can be used, each having different characteristics with respect to the molecule species they are able to capture, thus enabling a total extraction profile of multiple species to be performed in a single step.

One aspect of the inventions provides solution-phase capture-particles and methods of using them in isolating analytes from a sample, said method comprising one or more of the following steps including contacting a sample comprising analytes with solution-phase capture-particles under conditions effective for said capture particles to selectively and optionally reversibly, trap analytes of a defined molecular mass or particle size, wherein said capture-particles comprise a molecular sieve material which is capable of trapping and optionally releasing an analyte of a defined particle size or molecular mass. Other aspects of the present invention, as described in more detail below, also employ specific capture-particles which non-reversibly trap analytes.

Samples

Any sample can be utilized without restriction, including biological fluids, such as blood, blood components, cerebral spinal fluid, lymph, cellysates, tissue lysates, stool, urine, lymph, ascites, semen, ocular vitreous, etc.; environment samples, such as soil samples or extracts, ocean, pond, or river waters; water tower and drinking water samples; samples from chemical synthetic reactions; food samples; food processing samples (eg., from poultry processing plants), etc. For example, the methods can be used to detect contaminants in food, drinking water, and environment samples.

Analytes

The term “analyte” refers to any molecule of interest, including, organic molecules, inorganic molecules, polypeptides, carbohydrates, nucleic acids, lipids, derivatives thereof, and combinations thereof. Analytes include biomolecules which are shed from cell surfaces, released from cells (e.g., by exocytosis, lysis, etc.), metabolites, degradation products, protease digestion products, etc., without limitation. In one aspect of the invention, the methods can be utilized to entrap molecules in a biological fluid of a low molecular weight, especially those that would be excluded from the body by normal glomerular (kidney) filtration (e.g., molecules less that 30,000 Daltons) which are soluble and free-floating in the fluid or which are associated with carrier proteins. In general, the present invention can be used to capture any analyte of interest whose detection is desired including but not limited to sizes less than about 60,000 Da, less than about 50,000 Da, less than about 40,000 Da, less than about 30,000 Da, less than about 20,000 Da, less than about 10,000 Da, less than about 8,000 Da, less than about 6,000 Da, less than about 4,000 Da, less than about 2,000 Da, less than about 1,000 Da, including all individual values within each stated range.

With respect to body fluids, the capture-particles of the present invention can also be used to detect exogenous molecules, i.e., a molecule that was introduced into the body of the subject from whom the sample was obtained. Exogenous molecules can be actively or passively introduced into the subject. Examples of exogenous molecules include molecules present in, or in the form of, drugs, foods, tobacco, environmental products and contaminants (e.g., pesticides, carbon monoxide, etc), and essentially any molecule that enters the subject body through any route. Exogenous molecules also include their metabolites, by-products, and degradation products as processed or transformed in the body.

The capture particles can be utilized in any environment, including in vivo, ex vivo, and in vitro. For example, the particles can also be used as a tool to clear toxins from the blood in an in vivo or ex vivo context. For example, the particles can be utilized to remove toxic wastes from the blood, such as creatinine and urea, replacing the need for conventional dialysis.

Molecular Sieve Material

The capture-particles of the present invention can be comprised of a molecular sieve material (or molecular sieve portion). By this, it is meant that the material is porous, lattice-like, honeycombed, or has other properties that permit passage of analytes of a defined molecular mass or weight while excluding others. The size of the sieve pore is a determinant of whether the analyte can penetrate the capture-particle. The particle, itself, can be of any suitable size, e.g., less than about 10).Im, between about 10).Im and about 1).Im, between about 1).Im and about 100 nm, between about 1 nm and 100 nm, between about 5 nm and about 50 nm; between about 10 nm and about 20 nm; between about 10 nm and 1 nm; including all individual values within each recited range.

Pores in the sieve material can be designed based on the provided methods to diameters necessary for exclusion of unwanted molecules. Average pore sizes of between about 2 to about 20 nm, 1 nm to 1 f,Im, 1 nm to 10 nm, 1 nm to 50 nm, 10 nm to 50 nm, 50 nm to 100 nm, 10 nm to 200 nm, 50 nm to 500 nm, 1 nm to 10 nm, 1 nm to 5 nm, and other ranges are envisioned.

An optional feature of capture-particles is its ability to “trap” an analyte once it has entered the sieve material. The trapping may be achieved by using sieve materials which are capable of contracting and/or expanding in response to a physical or chemical treatment. For example, materials can be utilized which, when subjected to a chemical or physical treatment, contract or shrink, thereby trapping the analyte inside. Such materials can also be referred to as “smart materials” which have the ability to change shape or size by subject to a physical or chemical treatment. Any material having this property can be utilized without restriction, including, but not limited to, e.g., polyacrylamide and derivatives thereof; poly(N-isopropylacrylamide (e.g., Jones and Lyon, Macromolecules, 36:1988-1993, 2003; Jones and Lyon, Macromolecules, 33:8310-8306, 2000) and other N-alkyl substituted acrylamides; poly(N-vinylalkylamides); poly(methacrylic acid); poly(benzyl glutamate); poly(2-ethylacrylic acid); poly(4-vinylpyridine); ferroelectric liquid crystalline elastomers; piezoelectric polymers; “smart” gels, ceramics, alloys, and polymers, etc. See, also, e.g., Galaev et at., Pages 835-849; Zentel; Pages 850-860; Harrison and Ounaies, Pages 860-873; in Encyclopedia of Smart Materials, Volumes 1-2, Edited by, Schwartz, Mel© 2002 John Wiley & Sons. The capture-particles can be prepared routinely as known in the art or described in any of the above-mentioned references.

In one embodiment of the present invention the capture-particles do not contain any poly(N-isopropylacrylamide) constituent. Furthermore, capture particles in this embodiment also exclude poly(N-isoproplyacrylamide-co-acrylic acid.)

Physical or Chemical Treatment of Sieve Material

Physical and/or chemical treatments that can be utilized to contract and/or expand the sieve material can comprise thermal, electrical, magnetic, ultrasound, pressure, radiant, laser, osmotic, pH, salt, enzymatic, oxidation/reduction, dehydration/rehydration, ultraviolet, radiation, high intensity red light, treatments.

The sieve material can reversibly or non-reversibly contract or shrink. For example, the capture-particles can be placed in a solution where the analytes are permitted to penetrate, and then non-reversibly shrunk to capture the analyte. This could be useful where the objective is to remove a contaminant from a solution, and it is not necessary to analyze or further evaluate the nature of the captured analyte, thus not requiring it to be expanded. Alternatively, non-reversible capture-particle can be broken apart by sonication or other disruptive forces which destroy the integrity of the particle.

In one embodiment the capture-particle is capable of expanding and contracting to allow for capture and/or sequestration of an analyte.

In another embodiment, the capture-particle does not expand or contract to any significant degree to enable increased or reduced uptake of an analyte. That is the volume of the particle is substantially fixed. Examples of such capture particles include particles comprising viral proteins, Clatherin, carbon nanotubes or species which do not permit the expansion/contraction described previously. An example illustrating preparation of a polygonal structure from Clatherin is described in Jaarsveld, et al., Biochemistry 1981, 20, 4129-4135 hereby incorporated by reference.

Analyte Binding (Affinity) Portion

The capture particles can comprise surface protein properties for selective analyte binding and/or can be modified by the attachment of moieties that confer such binding properties.

The capture-particles can further comprise an analyte binding, affinity ligand or “bait.” Such terms can refer to substances which are capable of specifically attaching to an analyte of interest. Typical examples include, but are not limited to antibodies and derivatives thereof (e.g., Fab fragments and single-chain antibodies); binding proteins (e.g., receptors or fragments thereof for specific ligands); binding pairs (such as streptavidin/biotin); substrates; metals; chelating agents; nucleic acids; aptamers; enzyme-binding pockets; lectins; and/or an affinity group that is specific for an analyte of interest. The term “specific” has a functional meaning that the affinity ligand can be use to selectively bind to an analyte of interest in a sample and distinguish it from non-target analytes. It is specific in the sense that it can be used to detect analytes above background noise (“non-specific binding”). The affinity ligand can be selected such that it has a higher affinity for the analyte of interest than other components in the sample, allowing to out-compete any native binding proteins for the analyte.

The affinity ligands can be associated with the capture-particle in any suitable way. For example, they can used as a nucleus around which the sieve material is overlayed or deposited/nucleated in order to form the capture-particle; they can be directly incorporated into the sieve material prior to forming the particle (i.e., where the ligand is a component of the sieve material); they can be conventionally coupled (covalently or noncovalently) to the pore surfaces of the sieve material; etc. The affinity ligands can also be loaded into the capture particle by expanding the sieve material through appropriate physical or chemical treatment to reach a porosity that is large enough to admit the ligand, and then contacting the sieve material with the ligand under conditions effective for it to enter the particle. Once the particle is loaded with the affinity ligand, it can be shrunk by appropriate physical or chemical treatment, thereby reducing the sieve material's porosity, such that target analytes are still able to penetrate the particle, but larger analytes are excluded. The sieve porosity can be reduced after the affinity ligand loading step to pore size which is small enough to block the affinity ligand from diffusing out, making it unnecessary to link the affinity ligand to the sieve material. However, if desired, coupling processes can be used to link it to the sieve material.

Capture-particles baited with affinity ligands provide an analyte selection step, in addition to selection for analyte size or mass. For example, a capture-particle can be expanded to allow analytes to penetrate into it, and then the analytes can be further selected by their ability to specifically bind to an affinity ligand associated with the capture-particle. After the binding step is achieved (e.g., after equilibrium is reached), the particles can be separated and subjected to washing steps to remove unbound non-target analytes, and then optionally shrunk by a chemical or physical treatment.

The capture-particles can also further comprise antibodies as an affinity portion. Other candidate affinity portions include, but are not limited to, soluble receptors, polyamine analogs, antisense oligonucleotides, RNAi polynucleotides, ribozymes, and the like. Antibodies and soluble receptors are of particular interest as affinity portions where they target analytes of interest.

Antibodies

Affinity portions include antibodies and functional equivalents thereof that specifically bind to analytes. “Immunoglobulin” and “antibody” are used interchangeably and in their broadest sense herein. Thus, they encompass intact monoclonal antibodies, polyclonal antibodies, multispecific antibodies (e.g., bispecific antibodies) formed from at least two intact antibodies, and antibody fragments, so long as they exhibit the desired biological activity.

The variable domains of the heavy and light chain of an antibody recognize or bind to a particular epitope of a cognate antigen. The term “epitope” is used to refer to the specific binding sites or antigenic determinant on an antigen that the variable end of the immunoglobulin binds. Epitopes can be linear, i.e., be composed of a sequence of amino acid residues, conformational, such that an immunoglobulin recognizes a 3-D structure, or a combination thereof.

Monoclonal and Polyclonal Antibodies

Immunoglobulins of the invention may be polyclonal or monoclonal, and may be produced by any of the well known methods in this art.

Polyclonal antibodies are preferably raised in animals by multiple subcutaneous (sc), intraperitoneal (ip) or intramuscular (im) injections of the relevant antigen and an adjuvant. It may be useful to conjugate the relevant antigen to a protein that is immunogenic in the species to be immunized, In addition, aggregating agents such as alum are suitably used to enhance the immune response.

The term “monoclonal antibody” refers to an antibody obtained from a population of substantially homogeneous antibodies. Monoclonal antibodies are highly specific, being directed against a single antigenic site. Furthermore, in contrast to polyclonal antibody preparations that typically include different antibodies directed against different determinants, each monoclonal antibody is directed against a single determinant on the antigen.

In addition to their specificity, monoclonal antibodies are advantageous in that they may be synthesized while uncontaminated by other immunoglobulins. For example, monoclonal antibodies may be produced by the hybridoma method or by recombinant DNA methods. Monoclonal antibodies also may be isolated from phage antibody libraries.

Antibody Fragments

“Antibody fragments” comprise a portion of an intact antibody, preferably the antigen-binding or variable region thereof. Examples of antibody fragments include Fab, Fab′, F(ab′)2, Fv fragments, diabodies, linear antibodies, single-chain antibody molecules, and multispecific antibodies formed from antibody fragments.

Various techniques have been developed for the production of antibody fragments. Traditionally, these fragments were derived via proteolytic digestion of intact antibodies. Two digestion methodologies that are well known in the art include papain digestion and pepsin treatment. Antibody fragments may now additionally be produced directly by recombinant host cells.

Bispecific Antibodies

Bispecific antibodies of the invention are small antibody fragments with two antigen-binding sites. Each fragment comprises a heavy-chain variable domain connected to a light-chain variable domain in the same polypeptide chain. By using a linker that is too short to allow pairing between the two domains on the same chain, the domains are forced to pair with the complementary domains of another chain and create two antigen binding sites.

Methods for making bispecific antibodies are well known in the art. Traditional production of full length bispecific antibodies is based on the coexpression of two immunoglobulin heavy chain-light chain pairs, where the two chains have different specificities. Bispecific antibodies, however, may also be produced using leucine zippers.

The capture-particles can also further comprise detectable labels. By the term “detectable label,” it is meant any moiety or substance that can be detected by any means. These include, quantum dots, fluorescent labels, enzymes, magnetic particles, etc. The detectable label can be associated with any region of the capture-particle, including its pores and exterior surface. Detectable labels are useful in a number of ways, including for sorting different classes of capture-particles. For example, different classes of capture-particles can be produced, where each class possesses a different characteristic (e.g., a different pore size and/or a different affinity-ligand), and each carries a different detectable label associated with each class of particles. This enables the property of the particle class (e.g., able to bind to a specific antigen) to be identified by determining which detectable label it bears, For instance, a particle with a single chain antibody for PSA can be labeled with FITC, and a particle containing an antibody for (alpha)-Methylacyl-CoA racemase (AMACR) can be labeled with TRITC. After performing the entrapment step, the particles can be sorted by flow cytometry using fluorescent-activated cell sorting, separating the HA containing particles from the AMACR-containing particles.

Purification Methods

The capture particles of the current invention may be used in purification protocols to isolate analytes of interest from samples. As described above, the capture particles allow for purification of analytes based on size and affinity and this invention allows for quick isolation of analytes of interest from samples in order to preserve and study the analytes of interest. These analytes are preserved in the capture particles in order to prevent degradation from enzyme or other molecules in the sample.

Diagnostic Methods

The current invention also include a method of diagnosing a disease by contacting a sample comprising analytes with solution-phase capture-particles under conditions effective for the capture-particles to selectively bind analytes of a defined molecular mass, particle size, or defined affinity and then identifying the analytes selectively bound to the capture particles. The presence of analytes in the sample at identified concentrations would be characteristic of a disease state. Detecting the presence of an analyte could be done using methods well known to one of skill in the art such as enzyme-linked immunosorbant assay (ELISA), mass spectrometry, radioimmunoassay (RIA), micro array methods, immunoflourescence. northern blots, polymerase chain reaction (peR), and in situ hybridization.

Kits

In certain kit embodiments, the capture particles are provided in a form suitable for use in purification or diagnostic methods. Kits generally provide the capture particles as well as reagents, instructions, and the necessary products for performing the purification or diagnostic method. These kits are envisioned for use by doctors in a medical setting to store samples or by others to begin purification and isolation of serum analytes.

The disclosure of all publications cited above are expressly incorporated herein by reference in their entireties to the same extent as if each were incorporated by reference individually.

In some embodiments the capture-particles comprise a molecular sieve portion and an analyte binding portion wherein the molecular sieve portion, analyte binding portion or both further comprise a cross-linked region having modified porosity.

In some embodiments, the capture particles comprise a molecular sieve portion and an analyte binding portion wherein the molecular sieve portion, analyte binding portion or both comprise pore dimensions sufficient to exclude molecules larger than about 60 kDa.

In one embodiment, said analyte binding portion comprises at least one type of moiety capable of chemically or electrostatically binding or sequestering a analyte. Accordingly, the analyte is effectively retained in a region within the capture-particle. Forces between the analyte and the analyte binding region may be that of, covalent bonding, van der waals forces, hydrophobic-hydrophobic, hydrogen bonding, hydrophylic attraction, ionic attraction, or any combination thereof.

In another embodiment, the capture particles comprise pore sizes of between about 2 and about 20 nanometers with all individual values in between.

another embodiment, the capture particles comprise pore sizes of less than about 100 nm including all individual values within this range.

In another embodiment, the capture particle comprises pore sizes dimensioned to exclude molecules having sizes greater than about 60 kDa.

In another embodiment, the capture particle comprises pore sizes dimensioned to exclude albumin.

In another embodiment, the capture particle comprises pore sized sufficiently large to permit passage of molecules of 1404 Da size while excluding albumin, molecules having sizes greater than about 60 kDa or both.

The entire disclosure of all applications, patents and publications cited above, and in the figures are hereby incorporated by reference in their entirety. Certain embodiments of the invention are set forth in the non-limiting examples below. It will be apparent to one of skill in the art that there are other embodiments not explicitly set forth in this specification that are within the scope and spirit of the invention as claimed.

The examples described herein are illustrative of the present invention and are not intended to be limitations thereon. Different embodiments of the present invention have been described according to the present invention. Many modifications and variations may be made to the techniques described and illustrated herein without departing from the spirit and scope of the invention. Accordingly, it should be understood that the examples are illustrative only and are not limiting upon the scope of the invention.

EXAMPLES Example 1 Capture Particles Incorporating N-Isopropylacrylamide (NIP Am)

Capture particles incorporating N-Isopropylacrylamide (NIPAm) and N,N methylenebisacrylamide (BIS) were created by surfactant-free precipitation polymerization. BIS was used as the crosslinker, and the BIS:NIP Am monomer ratio determined the resultant network density and thus the average pore size. Further, a preparation of particles containing acrylic acid (AAc) was fabricated in order to incorporate a charge-based affinity bait into the particles. N-Isopropylacrylamide (NIPAm), N,N′-methylenebisacrylamide (BIS), ammonium persulfate (APS), acrylic acid (Mc) were purchased from Sigma-Aldrich of St. Louis, Mo. Water for reactions, washing and loading will be purified with a Millipore Milli-Q water purification system to a resistance of 18 MQ and passed through a 0.2).Im filter.

The total monomer concentration (NIPAm and BIS) was 0.3 M. Particles were made using varying amounts of crosslinker during polymerization, including 2% and 5% total concentration of crosslinking agent in order to vary the pore sizes of the particles. The monomers were fully dissolved in 190 mL of water inside of a round bottom 250 mL 3-neck flask fitted with a condenser and thermometer at a medium stir rate (magnetic stirrer). The solution was heated to 70° C. over the period of 1 hour under a stream of nitrogen. When a stable maximum stir rate was achieved, the polymerization was initiated with a 1.0 mL solution of 6 mM APS. The reaction was allowed to proceed for 3 hours under nitrogen. After cooling to room temperature overnight, 0.5 mL aliquots of the micro gel solution was placed into individual 1.5 mL capacity centrifuge tubes and diluted with 1.0 mL of water. The samples were then centhfuged for 20 minutes at 23° C. and 16,100 rcf with an Eppendorf 541 SR centrifuge. The supernatant was decanted and the microgels redispersed in water, again to a volume of 1.5 mL. This process was repeated for a total of five concentration/redispersion steps. Uniformity and size range was assessed using photon correlation spectroscopy (PCS submicron particles analyzer, Beckman Coulter), Atomic Force Microscopy (AFM), light microscopy as well as uptake of fluorescent dyes with fluorescence microscopy visualization. Flow cytometry also enabled relative size to be assigned through the use of commercially available fluorescently labeled sizing particles as standards.

In order to investigate the molecular exclusion properties of the particles, particles fabricated using 2% crosslinker concentration were incubated with five molecular species: FITC (MW 389), fluorescein linked to a small peptide angiotensin II (MW1404), FITC linked to insulin (MW 3500), to streptavidin (MW 53000), and to albumin (MW 66000). In-solution separation of five types of molecules was conducted. For each of the five fluorescent molecules, 0.1 ml of purified microgels were placed into a 1.5 mL centrifuge tube. To this, 0.1 mL of molecule solution was added and mixed gently on a vortex. Fluorescence uptake by the particles was measured using a F ACScan (Becton Dickinson). Experiments were conducted at different incubation times and at different concentrations of fluorescent molecules. These experiments indicated that small FITC molecules readily migrated into the particles, in as little as 10 minutes, and that the response is dose dependent. The fluorescein-labeled peptide also migrated into the particle, but with a less intense signal shift when compared with FITC, indicating that the particles have a size-mediated selectivity. For both FITC- and fluorescein-labeled peptide, the level of internalization was higher in the 2% crosslinker population of particles than in the 5% crosslinker population. This is consistent with a smaller nanopore size within the more highly crosslinked particle population, which would make internalization of the peptide more difficult. In both the 2% and 5% populations, albumin was excluded. Streptavidin and BSA were excluded from particles since there was no shift in the fluorescence signal. FITC labeled insulin was investigated both as an aqueous solution and spiked in human serum. Particles incubated with serum had a shift in the fluorescent signal that demonstrated insulin harvesting from a complex biological solution. Particles incubated with aqueous solution of FITC labeled insulin yielded a more intense fluorescent shift when compared to the serum.

SDS PAGE experiments were carried out on particles with a crosslinker concentration of 2% and demonstrated insulin (MW 3500) and myoglobin (MW 17000) uptake, BSA (MW 66000) exclusion. Acrylic acid functionalized particles were incubated with a 20 mM solution of myoglobin and captured all the protein in solution, giving a much higher uptake yield when compared to plain particles.

Example 2 Electro-Transport of the Particles

Serum incubated particles with 2% crosslinker were loaded in a sample tube of centrilutor micro-electroeluter (Millipore) where a 5 mm long 30% acrylamide/bis gel slice was previously polymerized. When an electric field was created, particles migrated towards the positive electrode through the gel slice without losing their protein content.

Example 3 Hydrogel Particles

The ability of hydrogel particles to perform directly, in one step and in solution, the partition, affinity separation, concentration, and stabilization of low molecular weight proteins in serum was analyzed as a new rapid method for blood derived biomarker isolation and analysis. Hydrogels, by definition, are three-dimensional cross-linked polymeric networks that can imbibe large amounts of water (Pelton, R. Adv Colloid Inteiface Sci 2000, 85, (1), 1-33). They are usually formed through monomer polymerization in the presence of a cross-linking agent, which is typically a monomer with at least two polymerizable functional moieties. Gels can be categorized as nonresponsive (simple polymeric networks dramatically swell upon exposure to water) or responsive gels (have added functionality and display changes in solvation in response to certain stimuli such as temperature (Li and Tanaka, The Journal of Chemical Physics 1990, 92, (2), 1365-1371) pH, (Jones and Lyon, Macromolecules 2000, 33, (22), 8301-8306; Moselhy et al., Journal of Biomaterials Science, Polymer Edition 2000, 11, (2), 123-147) ionic strength (Duracher et al., Colloid & Polymer Science 1998, 276, (3), 219-231; Duracher et al., Colloid & Polymer Science 1998, 276, (10), 920-929) light (Sershen et al., Temperature-sensitive polymer-nanoshell composites for photothermally modulated drug delivery, In 2000; Vol. 51, pp 293-298; Suzuki and Tanaka, Nature 1990, 346, (6282), 345-347) and electric field (Tanaka et al., Science, 1982, 218, 467-9).

Poly (N-alkyl acrylamides) have been extensively studied with respect to their thermoresponsivity (Pelton, R. Adv Colloid In teiface Sci 2000, 85, (1), 1-33; Inomata et al., Macromolecules, 1990, 23, 4887-8) with poly(N-isopropylacrylamide) (NIPAm) being one of the most strongly explored temperature sensitive hydro gels within this group. NIP Am containing particles are highly appealing for their potential biotechnological applications, because of their stability, uniformity, and versatility with regard to the ease of making physical-chemical modifications in the particles. NIP Am particles have been investigated for drug delivery slow release and targeted release, for solute desorption (Kawaguchi et al., Colloid & Polymer Science 1992, 270, (1), 53-57; Achiha et al., Polym. Adv. Technol, 1995, 6, (7), 534-540; Delair et al., Colloids and Surfaces A: Physicochemical and Engineering Aspects 1999, 153, (1-3), 341-353; Mattiasson et al., Nat. Protocols 2007, 2, (1), 213-220; Spamacci et al., J Biomater Sci Polym Ed 2005, 16, (12), 1557-74; Haruyuki Hiratani, Macromolecular Bioscience 2005, 5, (8), 728-733; Nahar et al., Crit Rev Ther Drug Carrier Syst 2006, 23, (4), 259-318; Wu et al., Journal of Controlled Release 2005, 102, (2), 361-372; Zhang et al., Biomaterials 2005, 26, (16), 3299-309; Woo et al., Pharm Res 2001, 18, (11), 1600-6; Basinska, Macromol Biosci 2005, 5, (12), 1145-68), interaction with cells (Achiha et al., Polym. Adv. Technol, 1995, 6, (7), 534-540), and coupling with oligodeoxyribonucleotides (OND) as a solid phase for hybridization (Delair et al., Colloids and Surfaces A: Physicochemical and Engineering Aspects 1999, 153, (1-3), 341-353). Since the size and porosity can be controlled by temperature, the use of temperature treatment to control uptake and release of chemicals has been one of the most extensively characterized application of NIP Am particles as vectors for controlled drug delivery (Spamacci et al., J Biomater Sci Polym Ed 2005, 16, (12), 1557-74; Haruyuki Hiratani, Macromolecular Bioscience 2005, 5, (8), 728-733; Nahar et al., Crit Rev Ther Drug Carrier Syst 2006, 23, (4), 259-318; Wu et al., Journal of Controlled Release 2005, 102, (2), 361-372; Zhang et al., Biomaterials 2005, 26, (16), 3299-309; Woo et al., Pharm Res 2001, 18, (11), 1600-6; Basinska, Macromol Biosci 2005, 5, (12), 1145-68).

In the present study, hydrogel particles containing an affinity bait and a defined porosity were developed and demonstrated to a) rapidly and in one step sequester the low molecular weight fraction of serum proteins, peptides and metabolites, b) remove and concentrate the target molecules from solution, and c) protect captured proteins from enzymatic degradation.

NIP Am based particles have been chosen because their high water content, broad range of tunable porosities, consistency and uniformity following synthesis, functional reconstitution following freeze-drying, and potential biocompatibility. By changing the percentage of cross linking agent and temperature, it is possible to control the particles size and the effective porosity. A significant advantage for the application studied here is the ability of these particles to rapidly uptake molecules because of their open structure, high water content, dual hydrophobic and hydrophilic chemical moieties that can be substituted in the polymer, and large surface area. This is a critical requirement for the goal of rapid harvesting of labile small proteins in solution and protecting the proteins from degradation. The small size, uniformity of particle dimension, and reproducibility from batch to batch, of NIP Am provide special advantages for applications in flow cytometry.

Example 4 Hydrogel Particle Synthesis and Characterization

Gel particles incorporating N-isopropylacrylamide (NIP Am) were created and evaluated for molecular sieving properties. A second class of particles containing both NIP Am and acrylic acid (AAc), NIPAm/AAc, were fabricated to incorporate a charge based affinity bait into the particles, as shown in FIG. 1 (Pelton, Adv Colloid Interface Sci 2000, 85, (1), 1-33; Jones and Lyon, Macromolecules 2000, 33, (22), 8301-8306; Saunders and Vincent, Advances in Colloid and Interface Science 1999, 80, (1), 1-25).

To obtain N-isopropylacrylamide (NIP Am) particles, NIPAm (1.4 g) and BIS (0.04 g) were dissolved in 150 ml of water and then filtered twice through a membrane filter (Pall Gelman Metricel). The solution was degassed under vacuum for at least 20 minutes. SDS (0.057 g) was then dissolved in the monomer solution, which was filtered again. During filtration 40 ml of water were used for transfer and washing. The solution was placed in a round bottom 250 ml 3-neck flask fitted with a condenser and thermometer at a medium stir rate (Coning magnetic stirrer). The solution was heated to 70° C. for 1 hour under a nitrogen atmosphere. A stable maximum stir rate was reached and polymerization initiated via addition of APS (0.069 g) dissolved in 10 ml of degassed water. The reaction was allowed to proceed at a temperature of 70° C. for 6 hours under nitrogen. NIP Am/acrylic acid (AAc) particles were fabricated using the same reaction condition as NIP Am particles above. The initial monomer solution was obtained by dissolving NIPAm (1.3 g), BIS (0.10 g), and Mc (0.072 g) in 150 ml water. All particles were purified via dialysis (Spectra/Por 7 dialysis membranes, MWCO 10,000, VWR) against frequent changes of stirring water for 2 weeks at 4° C.

Example 5 Particle Size Dependence on Temperature and pH

Particle size dependence on temperature and pH were determined via Photon Correlation Spectroscopy (PCS, Submicron Particle Size Analyzer, Beckman Coulter). Average values were calculated for 3 measurements using a 200 second integration time, and the solutions were allowed to thermally equilibrate for 10 minutes before each set of measurements. Measured values were then converted to particle sizes via the StokesEinstein relationship (Pecora, Dynamic Light Scattering: Applications of Photo Correlation Spectroscopy. Springer: 1985; p 436). NIPAm particle size decreased with increasing temperature (FIG. 2), which is a distinctive characteristic of thermo responsive hydrogels (Spamacci et al., J Biomater Sci Polym Ed 2005, 16, (12), 1557-74; Haruyuki Hiratani, Macromolecular Bioscience 2005, 5, (8), 728-733; Nahar et al., Crit Rev Ther Drug Carrier Syst 2006, 23, (4), 259-318; Wu et al., Journal of Controlled Release 2005, 102, (2), 361-372; Zhang et al., Biomaterials 2005, 26, (16), 3299-309; Woo et al., Pharm Res 2001, 18, (11), 1600-6). The NIPAmI Mc particles showed a similar temperature dependence with respect to particle size, however they also demonstrated a pH dependent behavior (FIG. 2). At low pH (3.5) Mc groups are protonated and NIP Ami Mc particle size dependence on temperature is similar to underivatized particles. At higher pH (4.5 and 6.5) AAc groups are partially deprotonated and the average particle size increases, likely due to Coulombic interaction between polymeric chain and osmotic pressure resulting from counter ion ingress in particles (Fernandez-Nieves et al., Macromolecules 2000, 33, 2114-2118; Ito et al., Langmuir 1999, 15, (12), 4289-4294).

Particles were further characterized by atomic force microscopy (AFM) using an NSCRIPTOR™ DPN● System (NanoInk). Images were acquired under AC mode using a silicon tip with a typical resonance frequency of 300 kHz and a radius smaller than 10 nm. Aliquots of 196 w/v particles (50 f.IL) were deposited on freshly cleaved mica; samples were incubated for ten minutes in humid atmosphere at room temperature to allow deposition, and then dried under nitrogen flow. AFM images of these particles (FIG. 2) show them to be homogeneous in size, and with particle diameters consistent with those measured with light scattering.

Example 6 Molecular Sieving by Hydrogel Particles

NIP Am particles were tested for their molecular sieve performance in solution as schematically presented in FIG. 3; the goal being to create particles that could capture proteins and small molecules with molecular weights less than 20,000 Da since the peptidome is thought to contain a rich source of biomarkers (Tirumalai et al., Molecular & cellular proteomics 2003, 2, (10), 1096-103; Merrell et al., Journal of biomolecular techniques 2004, 15, (4), 238-48; Orvisky et al., Proteomics 2006, 6, (9), 2895-902).

This size range contains informative proteins, peptides and metabolites that are difficult, if not impossible, to separate from complex protein mixtures (such as serum or plasma) with adequate yield using 2-D gel electrophoresis or column chromatography. The degree of cross-linking within the particle enabled exclusion of albumin and other high abundance large molecules while capturing molecules with sizes smaller than the cut-off pore size of the particles. Particles with varied degrees of cross-linking were investigated until one was identified that demonstrated an effective 20,000 Da exclusive pore size. These particles were further studied in order to evaluate their sieving efficiency and nonspecific binding of excluded molecules to the particle surface. Because serum albumin is present in large excess (106-109 fold) relative to the proteins and peptides of interest, it was necessary to examine the efficiency and completeness of albumin exclusion.

Two independent methods were used to measure sieving performance: flow cytometry and gel electrophoresis. Aliquots of NIP Am particles (50).IL, 10 mg/mL) were incubated with target molecular species, and centrifuged to collect the particles (7 minutes, 25° C., 16,100 rcf). The supernatant was removed and the particles were resuspended in 1 mL water. Centrifugation and washing were repeated three times and the fluorescent intensity of the particles was measured using a F ACScan flow cytometer (Becton Dickinson). The background fluorescent signal of untreated particles in water was used as a reference for all measurements. Fluorescein isothiocyanate (FITC, MW 389 Da) was used as a model to study small molecule uptake and the dependence of uptake on incubation time and concentration. Particles incubated with various concentrations of FITC (5).IM, 20).IM, and 100).IM) showed a dose dependent uptake rate (FIG. 4) toward saturation. Time course studies demonstrated that FITC uptake could occur rapidly (5 minutes, FIG. 4) at 10% v/v particles concentration.

As shown in FIG. 5 particles incubated with FITC-BSA (MW 66,000 Da) have no detectable shift in fluorescence signal relative to the particle background fluorescence, which indicates no detectable BSA uptake or non specific binding by the particles. On the other hand, incubation with FITC-insulin (MW 3,500 Da) results in a right shift in fluorescence relative to the control, confirming the uptake of insulin by the particles. FITC alone (MW 389 Da), a molecule in the size range of many metabolites, and FITC-myoglobin (MW 17,000 Da), another protein below the effective size cut-off of the particles, were both rapidly captured.

These findings were confirmed by SDS-PAGE analysis. The particles were directly loaded on the gel after incubation with protein solution and washing. Insulin (FIG. 5), and myoglobin (FIG. 5) were trapped by particles, while BSA was totally excluded (FIG. 5).

Example 7 Incorporation of a Charged Bait in the Molecular Sieving Particles Significantly Enhances Uptake

Passive molecular sieving cannot effectively harvest and concentrate all of the target proteins in solution because the concentration of the captured target protein in the particles is dependent on the equilibrium between rates of proteins exiting and entering particles and the concentration of the target protein in the bulk solution. Consequently particles were constructed that incorporated an affinity bait to facilitate harvesting of target proteins and prevent the captured proteins from exiting the particle.

A negatively-charged moiety was selected as a bait for proteins and molecules that have a positive net charge. Incorporation of a negatively-charged bait within the particles would allow the particles to preferentially sequester and concentrate positively charged proteins, peptides and other biomolecules. Therefore, particles were prepared based on a NIP Ami AAc copolymer, which carries a large net negative charge at pH values greater than 3.5. As shown schematically in FIG. 6, the presence of charged bait, in principle, should enhance substantially the Keq and thereby achieve a significantly higher concentration of the target protein inside the particle compared to the solution outside the particle.

As shown in FIG. 7, NIP Ami AAc particles concentrated analytes from solution with substantially greater efficiency relative to underivatized NIP Am particles. Suspensions of NIP Am and NIPAmIAAc particles (10 mg/mL) were incubated for 1 hour with myoglobin (MW 17,000 Da, 20).IM in water). Following incubation with NIPAm particles, significant levels of myoglobin remained in the bulk solution with some protein being bound by the particles, which lack the anionic affinity bait (FIG. 7). Following incubation with NIP Ami AAc particles, which contain the anionic affinity bait, all of the myoglobin had been captured by the NIP Ami AAc particles, with no detectable myoglobin remaining in bulk solution. Correlating myoglobin band intensity for serial dilutions of NIP Ami AAc particles with that of NIP Am particles suggests that the NIPAmIAAc particles sequestered myoglobin with more than 128-fold greater efficiency compared with particles that lack the affinity bait.

In order to demonstrate that the superior protein uptake associated with NIP Ami AAc particles was charge driven, aliquots of a solution containing myoglobin (20).IM) and BSA (20).IM) were incubated with NIP Am/AAc particles in phosphate buffer titrated to either pH 5.5 or pH 8 (FIG. 7). Particles were separated by centrifugation and washed three times with MilliQ water. At pH 5.5, myoglobin (pl 7) is expected to be positively charged, and electrostatic interactions between the protein and the negatively charged carboxyl groups of NIP Ami AAc particles would be attractive. However at pH 8, myoglobin would be negatively charged, and any electrostatic interactions with the anionic particles would likely be repulsive in nature. Consistent with these expectations, myoglobin was efficiently sequestered by NIPAm/AAc particles at pH 5.5 where the protein and the particles have opposite net charges, and no myoglobin was detectable in particles that had been incubated with myoglobin at pH 8 (FIG. 7).

The efficiency of NIP Am/AAc affinity baited particles to bind and concentrate proteins and peptides with MW less than ca. 20,000 Da is illustrated in FIG. 8. NIP Ami Mc and NIP Am particles were each incubated for 1 hour with lysozyme (20).IM) and BSA (20).IM) in Tris (pH 7.50 mM). The particles then were washed with three 1 mL volumes of water, and the captured proteins were electro-eluted onto an SDS polyacrylamide gel.

While the NIP Am/Mc particles appeared to have captured all of the lysozyme present in the solution, there was no indication that BSA had been bound non-specifically by the particles. As was observed with myoglobin, NIP Am particles, lacking the affinity bait, did not appear to significantly concentrate lysozyme.

A solution of protein molecular weight markers was used to further assess the molecular weight cut off (MWCO) of the proteins sequestered by the particles (FIG. 8). The solution consisted of 0.5 mg/mL of each of the following proteins: aprotinin (MW 6,500 Da, Sigma-Aldrich), lysozyme (MW 14,400 Da, Sigma-Aldrich), trypsin inhibitor (MW 21,500 Da, Invitrogen), carbonic anhydrase (MW 31,000 Da, SigmaAldrich), ovalbumin (MW 45,000 Da, Sigma-Aldrich), and BSA (MW 66,000 Da, Fisher Scientific) dissolved in Tris (PH 7, 50 mM). It was found that NIPAmIAAc baited particles, incubated with the protein solution, effectively captured and concentrated all protein molecules with MW less than ca. 21,500 Da, and did not bind any proteins with MW greater than 21,500 Da. NIP Am particles showed a similar MWCO with MW<=14,400 Da or smaller and not binding proteins MW>=14,400 Da. The MWCO resolution achieved with NIP Ami Mc and NIP Am particles compares favorably, or exceeds, that associated with standard molecular sieving chromatography 41. In order to further determine the molecular sieving properties of the beads, NIP Ami AAc particles were incubated with platelet derived growth factor B (0.003 mg/mL, 14,500 Da, Cell Signaling) and BSA (0.067 mg/mL) in Tris (100 mM pH 7) for one hour. Washing procedure was the same as described before. SDS PAGE in FIG. 9 shows complete PDGF uptake and BSA exclusion. PDGF is a representative model for low abundance low molecular weight protein present in the blood and PDGF-B concentration in blood is 3.3 ng/mL (Eppley et al., Plastic and reconstructive surgery 2004, 114, (6), 1502-842).

Because of the drastic change in size particles undergo when the temperature of solution is altered, temperature effects on MWCO were investigated. The solution of molecular weight markers described above was incubated with NIP Ami AAc particles at 25, 37, and 45° C. and the temperature was a factor that did not affect the MWCO (data not shown).

Example 8 Sequestration from Serum

Based on the above results, the ability of the particles to capture small molecules spiked in complex solutions such as serum was then tested to mimic real-world biomarker discovery and analysis type experiments. Aliquots of FITC-labeled insulin (final concentration 40 M) in 1:10 diluted serum were incubated with NIPAm and NIP Ami Mc particles. Flow cytometry analysis demonstrated that NIP Am particles incubated in serum containing FITC-insulin yielded a right shift in fluorescence intensity relative to control particles and particles incubated with serum alone (FIG. 10).

This result clearly demonstrated the ability of NIP Am particles to capture insulin from a complex matrix such as serum. However, the capture efficiency of the NIPAm particles incubated with a simple aqueous solution containing only insulin was lower than that attained with serum incubated NIP Am particles. While the two classes of particles exhibited a similar uptake of insulin in an aqueous solution, the particles with the charged bait were more efficient in capturing insulin spiked into serum compared to the underivatized particles. (FIG. 10).

Time courses uptake studies for NIP Am and NIP Ami Mc particles incubated with FITC-labeled insulin (pl 5.3) were conducted in order to confirm and extend the data obtained for the small molecule, FITe. Histograms of fluorescence intensity associated with Flow cytometry analyses of NIP Am and NIP Ami AAc particles incubated with FITC-labeled insulin collected at different time intervals are reported in FIG. 11. This data indicates that sequestration occurs rapidly (5 minutes) and constant over time.

Example 9 Rapid Time Course of Target Protein Uptake by Bait Containing Particles

In order to prove that the kinetics of protein uptake is very rapid, the amount of protein remaining in bulk solution after incubation with NIP Ami AAc particles was measured by Reverse Phase Protein Arrays (RPPA) (Gulmann et al., The Journal of pathology 2006, 208, (5), 595-606). RPPA was chosen as a means to determine protein concentration in particles supernatant since other methods like Bradford assays do not have sufficient sensitivity and our goal was demonstrate how complete the protein removal from bulk solution was. Different amounts of NIPAmIAAc particles (1.15 and 11.5 million) were incubated with lysozyme (20).IM) in Tris (pH 7, 50 mM) in a total volume of 100).IL for periods of 1 and 10 minutes. After centrifugation of the particles, aliquots of supernatant were spotted on a nitrocellulose coated slide (FAST slide, Whatman) using an Aushon 2470 robotic arrayer (Aushon Biosystems). Arrays were stained with a colloidal gold solution, AuroDye Forte Kit (Amersham), images were acquired using a Powerlook 1120 scanner (Umax), and numeric values were obtained from images with ImageQuant (GE Healthcare) and processed with SigmaPlot (Systat). The bulk solution after a one minute incubation with 1.15 million particles contained 28% of the initial protein amount, and 15% after ten minutes. Moreover, the solution recovered from incubation with 11.5 million particles after 1 and 10 minutes contained 5% and 9% of the initial amount, respectively (FIG. 12). It should be noted that, since in all the time course experiments the separation of particles from solution was obtained by centrifugation, reported time values refer to incubations time intervals only. Beyond that particles were in contact with solution for additional 7 minutes required for centrifugation.

The kinetics of protein uptake by NIP Ami AAc particles was further investigated by incubating particles with BSA (20).IM) and lysozyme (20).IM) in Tris (pH 7, 50 mM) at room temperature and using SDS-PAGE to monitor lysozyme uptake at time points of 1, 10, 20, 30, and 60 minutes (FIG. 12). The results of this experiment showed that lysozyme sequestration was nearly complete after 1 minute and was complete by 60 minutes, confirming that the process occurs very quickly as indicated in the flow cytometry time course study described above. As expected, BSA was excluded by the particles, and none of the BSA was taken-up by the NIPAmIAAc throughout the duration of the experiment (60 minutes).

Example 10 Demonstration of Isolation and Enrichment of Low Molecular Weight and Low Abundance Analytes from Serum

The ability of NIP AM and NIPAmI AAc particles to sequester and concentrate low concentration candidate protein biomarkers from serum for proteomic analysis was evaluated by incubating the particles with a 1:10 v Iv dilution of serum in water for 1 hour. The trapped proteins were electrophoretically eluted from the particles under denaturing conditions and then trypsin digested. The particles were heated in SOS sample buffer for 5 minutes at 100° C. and loaded on a 4-20% Tris Glicine gel (Invitrogen). Bands below 30 kDa were cut and in-gel trypsin digestion was performed (Camerini et al., Proteomics Clin. Appl. 2007, 1, 176-184). The resulting peptide fragments were analyzed by online liquid chromatographylelectrospray ionization tandem mass spectrometry (LC/ESI MS) using LTQ-Orbitrap mass spectrometer (Thermo Fisher). Reverse phase column was slurry-packed in-house with 5 m, 20 A pore size C18 resin (Michrom BioResources, CA) in 100 mm i.d.×10 cm long fused silica capillary (Polymicro Technologies, Phoenix, Ariz.) with a laser-pulled tip. After sample injection, the column was washed for 5 minutes with mobile phase A (0.1% formic acid) and peptides were eluted using a linear gradient of 0% mobile phase B (0.1% formic acid, 80% acetonitrile) to 50% mobile phase B in 50 minutes at 200 nl/min, then to 100% B in an additional 5 minutes. The L TQ mass spectrometer was operated in a datadependent mode in which each full MS scan was followed by five MS/MS scans were the five most abundant molecular ions were dynamically selected and fragmented by collision-induced dissociation (CID) using a normalized collision energy of 35%. MS/MS data were matched against the NCB I (National Center for Biotechnology Information) human protein database with the program SEQUEST (Bioworks software, Thermo) using full tryptic cleavage constraints. High-confidence peptide identifications were obtained by applying the following filters to the search results: cross-correlation score (XC orr)>=1.9 for 1+, 2.2 for 2+, 3.5 for 3+, and a maximum probability for a random identification of 0.01. The list of identified proteins in Table 1 and Table 2 demonstrated that albumin and other high abundance serum proteins were not present in the particles. On the other hand, the list of identified proteins indicates that the particles sequestered rare and small-sized serum proteins and peptides.

TABLE 1 Reference Accession P (pep) Sf Score MW complement 56786155.0 4.83E−12 3.43E+00 40.28 25757.13 component 1, q subcomponent, gamma polypeptide [Homo sapiens] complement 66347875.0 5.65E−12 2.72E+00 30.24 80147.95 component 1, r subcomponent [Homo sapiens] haptoglobin-related 45580723.0 1.12E−11 9.76E−01 10.22 39004.70 protein [Homo sapiens] PREDICTED: similar 113419208.0 1.12E−11 9.80E−01 10.22 11254.79 to Putative S100 calcium-binding protein A11 pseudogene [Homo sapiens] complement 67190748.0 1.12E−11 3.58E+00 40.24 192663.60 component 4A preproprotein [Homo sapiens] orosomucoid 1 9257232.0 1.12E−11 8.17E−01 10.13 23496.77 precursor [Homo sapiens] CD5 antigen-like 5174411.0 1.12E−11 3.80E+00 40.25 38062.96 (scavenger receptor cysteine rich family) [Homo sapiens] serum amyloid P 4502133.0 1.12E−11 4.15E+00 50.20 25371.13 component precursor [Homo sapiens] complement 87298828.0 1.12E−11 9.82E−01 10.26 26704.49 component 1, q subcomponent, B chain precursor [Homo sapiens] apolipoprotein A-I 4557321.0 1.12E−11 6.86E−01 10.12 30758.94 preproprotein [Homo sapiens] haptoglobin [Homo 4826762.0 1.12E−11 3.70E+00 40.21 45176.59 sapiens] complement 7705753.0 1.12E−11 8.24E−01 10.15 26000.19 component 1, q subcomponent, A chain precursor [Homo sapiens] platelet factor 4 4505733.0 1.12E−11 1.80E+00 20.16 10837.89 (chemokine (C—X—C motif) ligand 4) [Homo sapiens] immunoglobulin J 21489959.0 1.12E−11 9.45E−01 10.15 18087.00 chain [Homo sapiens] lysozyme precursor 4557894.0 1.12E−11 9.03E−01 10.15 16526.29 [Homo sapiens] transthyretin [Homo 4507725.0 1.12E−11 6.77E−01 10.13 15877.05 sapiens] dermcidin 16751921.0 1.12E−11 8.66E−01 10.13 11276.83 preproprotein [Homo sapiens] mesotrypsin 21536452.0 1.12E−11 9.37E−01 10.17 26680.18 preproprotein [Homo sapiens] alpha 1 globin [Homo 4504347.0 1.12E−11 9.62E−01 10.16 15247.92 sapiens] beta globin [Homo 4504349.0 1.12E−11 9.36E−01 10.17 15988.29 sapiens] hypothetical protein 91206438.0 1.12E−11 8.68E−01 10.18 22058.92 LOC649897 [Homo sapiens] complement 41393602.0 1.12E−11 9.25E−01 10.15 76634.85 component 1, s subcomponent [Homo sapiens] protein kinase C and 6005826.0 1.12E−11 8.23E−01 10.15 55870.13 casein kinase substrate in neurons 2 [Homo sapiens] PREDICTED: similar 89036176.0 1.12E−11 8.89E−01 10.14 36406.56 to Keratin, type II cytoskeletal 2 oral (Cytokeratin-2P) (K2P) (CK 2P) [Homo sapiens] platelet factor 4 variant 4505735.0 1.12E−11 8.70E−01 10.19 11545.28 1 [Homo sapiens] bromodomain 41350212.0 1.12E−11 8.63E−01 10.18 74092.27 containing 7 [Homo sapiens] SH3-domain binding 19923155.0 1.12E−11 2.64E−01 10.13 62220.29 protein 2 [Homo sapiens] zinc finger, CCHC 57863250.0 1.12E−11 8.14E−01 10.17 184587.10 domain containing 11 isoform c [Homo sapiens] apolipoprotein A-II 4502149.0 1.12E−11 8.90E−01 10.14 11167.90 preproprotein [Homo sapiens] heterogeneous nuclear 51477708.0 1.12E−11 6.31E−01 10.18 30653.14 ribonucleoprotein D isoform d [Homo sapiens] polo-like kinase 4 21361433.0 1.12E−11 6.16E−01 10.13 109016.40 [Homo sapiens] apolipoprotein L1 21735614.0 1.12E−11 6.63E−01 10.12 43946.95 isoform a precursor [Homo sapiens] coronin, actin binding 16554583.0 1.12E−11 9.33E−01 20.14 59697.38 protein, 2A [Homo sapiens] Table 1. Mass spectrometry analysis of proteins electroeluted from NIPAm particles after 1 hr incubation with 1:10 v/v dilution serum, P(pep) displays the probability value for the peptide, Sf displays the final score that indicated how good the protein match is, Score displays a value that is based upon the probability that the peptide is a random match to the spectral data, Accession displays a unique protein identification number for the sequence

TABLE 2 Reference Accession P (pep) Sf Score MW complement 56786155.0 3.55E−14 1.86E+00 20.30 25757.13 component 1, q subcomponent, gamma polypeptide [Homo sapiens] hypothetical protein 91206438.0 3.55E−14 2.90E+00 30.26 22058.92 LOC649897 [Homo sapiens] PREDICTED: similar 113419208.0 3.55E−14 1.46E+00 20.25 11254.79 to Putative S100 calcium-binding protein A11 pseudogene [Homo sapiens] apolipoprotein C-III 4557323.0 3.55E−14 9.79E−01 10.24 10845.50 precursor [Homo sapiens] pro-platelet basic 4505981.0 3.55E−14 5.61E+00 60.25 13885.42 protein precursor [Homo sapiens] complement 4557385.0 3.55E−14 9.80E−01 10.20 187045.30 component 3 precursor [Homo sapiens] small nuclear 4507129.0 3.55E−14 9.15E−01 10.19 10796.64 ribonucleoprotein polypeptide E [Homo sapiens] keratin 2 [Homo 47132620.0 3.55E−14 5.75E+00 70.21 65393.19 sapiens] albumin precursor 4502027.0 3.55E−14 9.28E+00 100.22 69321.63 [Homo sapiens] ribosomal protein 4506643.0 3.55E−14 9.73E−01 10.21 10268.48 L37a [Homo sapiens] complement 67190748.0 3.55E−14 1.91E+00 20.17 192663.60 component 4A preproprotein [Homo sapiens] A-gamma globin 28302131.0 3.55E−14 9.44E−01 10.14 16118.27 [Homo sapiens] platelet factor 4 4505733.0 3.55E−14 3.44E+00 40.18 10837.89 (chemokine (C—X—C motif) ligand 4) [Homo sapiens] PREDICTED: 113418327.0 3.55E−14 8.55E−01 10.19 31688.42 hypothetical protein [Homo sapiens] H4 histone family, 4504315.0 3.55E−14 1.51E+00 20.13 11360.38 member J [Homo sapiens] lysozyme precursor 4557894.0 3.55E−14 9.66E−01 10.20 16526.29 [Homo sapiens] mesotrypsin 21536452.0 3.55E−14 9.68E−01 10.18 26680.18 preproprotein [Homo sapiens] alpha 1 globin [Homo 4504347.0 3.55E−14 9.15E−01 10.14 15247.92 sapiens] fibrinogen, alpha 4503689.0 3.55E−14 8.35E−01 10.12 94914.27 polypeptide isoform alpha-E preproprotein [Homo sapiens] hypothetical protein 21361734.0 3.55E−14 6.53E−01 10.12 83244.77 LOC55683 [Homo sapiens] crumbs homolog 1 41327708.0 3.55E−14 6.87E−01 10.15 154080.40 precursor [Homo sapiens] PREDICTED: similar 41146739.0 3.55E−14 6.26E−01 10.15 41686.95 to glutamate receptor, ionotropic, N-methyl D-aspartate-like 1A isoform 1 isoform 1 [Homo sapiens] PREDICTED: similar 113419903.0 3.55E−14 7.75E−01 10.12 10194.18 to Neutrophil defensin 1 precursor (HNP-1) (HP-1) (HP1) (Defensin, alpha 1) [Homo sapiens] CDK5 regulatory 28872784.0 3.55E−14 9.05E−01 10.12 56187.84 subunit associated protein 1 isoform b [Homo sapiens] complement 87298828.0 3.55E−14 8.90E−01 10.15 26704.49 component 1, q subcomponent, B chain precursor [Homo sapiens] interferon-induced 31542980.0 3.55E−14 9.40E−01 10.22 55949.57 protein with tetratricopeptide repeats 3 [Homo sapiens] lamin A/C isoform 1 27436946.0 3.55E−14 8.73E−01 10.14 74094.81 precursor [Homo sapiens] double C2-like 6005997.0 3.55E−14 5.53E−01 10.13 45920.53 domains, beta [Homo sapiens] desmoglein 4 [Homo 29789445.0 3.55E−14 9.06E−01 10.13 113751.30 sapiens] cadherin EGF LAG 7656967.0 3.55E−14 1.56E+00 20.14 329276.70 seven-pass G-type receptor 1 [Homo sapiens] procollagen, type III, 4502951.0 3.55E−14 9.12E−01 10.15 138470.20 alpha 1 [Homo sapiens] ATPase, H+ 20357547.0 3.55E−14 8.61E−01 10.16 13361.95 transporting, lysosomal 14 kD, V1 subunit F [Homo sapiens] Table 2. Mass spectrometry analysis of proteins electroeluted from NIPAm/AAc particles after 1 hr incubation with 1:10 v/v dilution serum, P(pep) displays the probability value for the peptide, Sf displays the final score that indicated how good the protein match is, Score displays a value that is based upon the probability that the peptide is a random match to the spectral data, Accession displays a unique protein identification number for the sequence

Example 11 Protein Sequestration by Particle Blocks Protease Degradation

One of the major problems associated with biological fluids is the potential for sample degradation during collection, transport, storage and analysis. Endogenous clotting cascade enzymes, enzymes released from damaged cells, or exogenous enzymes (from contaminating bacteria) can contribute to the degradation of diagnostically important proteins, as schematically shown in FIG. 13.

The lack of standardized preservation methods could result in bias in high-throughput analysis of serum and plasma (Ayache et al., American journal of clinical pathology 2006, 126, (2), 174-84). While it was expected that proteases with MW greater than the MWCO of the particles (˜20,000 Da) would be excluded from the interior space of the particles and thereby denied access to captured proteins, smaller proteases such as trypsin (23,800 Da) are more likely to be able to enter the particles. Additionally, it was not known whether proteases that entered charged-bait particles would retain their enzymatic potency when both the substrate proteins and the enzyme were sequestered by the particles (FIG. 12). Therefore, NIP Ami AAc particles were incubated at 37° C. in a pH 7 NH4HC03 (100 mM) solution containing lysozyme (0.5 mg/mL) and trypsin (0.05 mg/mL, Promega). Trypsin was selected for these studies based on its small size and the fact that the tryptic digestion of lysozyme would produce very characteristic cleavage products. The conditions used in this experiment would allow both lysozyme and trypsin to enter the particle. Analysis of the captured proteins by SDS PAGE after incubation for 1 hour and overnight showed only two bands—one corresponding to trypsin and the other to the full length lysozyme, indicating that no degradation of the protein had occurred (FIG. 14). Incubation of lysozyme (0.5 mg/mL) with trypsin (0.05 mg/mL) at 37° C. in a pH 7 NH4HC03 (100 mM) solution in the absence of NIPAmIAAc particles resulted in degradation of lysozyme. SDS-PAGE analysis of the reaction after incubation for 1 hour and overnight clearly indicated the presence of low molecular weight peptide fragments, which showed that lysozyme was proteolyzed by trypsin in the absence of NIP Ami AAc particles. These results clearly indicate that sequestration of small proteins by affinity-bait particles can effectively shield bound proteins from proteases including those that are capable of entering the particles interior.

In order to better understand the benefits associated with sequestration of proteins by NIP Ami AAc affinity-bait particles, NIP Ami AAc particles were incubated at 37° C. with a combination of BSA (0.5 mg/mL), lysozyme (0.5 mg/mL) and trypsin (0.05 mg/mL) in 100 mM NH4HC03 (PH7). As with the previous protection study, the reaction was analyzed using SDS-PAGE after incubating 1 hr and overnight. In the absence of NIPAmIAAc particles, the majority of BSA had been digested after 1 hr and the band corresponding to full-length BSA had disappeared after incubating overnight (FIG. 14). As was noted earlier, the NIPAmIAAC particles efficiently sequestered both lysozyme and trypsin, and protected lysozyme from proteolysis by trypsin. However, the particles did not bind BSA, and the presence of low molecular weight bands in the supernatant after 1 hour and overnight incubation accompanied by the decrease in intensity of the band corresponding to full-length BSA indicates that BSA was not protected from degradation by trypsin. Suppression of proteolytic activity by enzymes small enough to enter the particles, such as trypsin, may occur because immobilization of the enzymes by the charge-bait particle prevents them from binding substrate proteins or may be the result of steric hindrance associated with trapping of the substrate by the affinity-bait groups in the particle thus preventing enzymes from productively binding target proteins inside the particle. Thus, the functional state of the proteins sequestered by the charge-bait may be similar to that of proteins arrested using a precipitating fixative treatment.

Even if products of enzymatic degradation were clearly shown in the above presented results, the unfolded state of lysozyme is known to contain region resistant to trypsin proteolysis (Noda et al., Biopolymers, 1994, 34, (2), 217-226). Therefore, incubation with particles was repeated with reduced and alkylated lysozyme in order to exclude any bias. Lysozyme was reduced by incubation with Dithiothreitol (DTT) (10 mM) in NH4HC03 buffer (50 mM, pH 8) containing urea (2 M) for one hour at room temperature. Iodoacetamide was added to the solution to a final concentration of 50 mM and let react in the dark for 30 minutes. Buffer was exchanged and protein washed with MilliQ water by means of Centricon centrifugal filter units (Millipore) with MWCO of 3,000 Da. Lysozyme was resuspended in NH4HC03 (pH 8,100 mM) to an estimated final concentration of 0.5 mg/mL; trypsin (0.05 mg/mL) and NIPAmIAAc particles were added and the solution was incubated for 1 hour at 37° C. Particles were washed as previously described and loaded on SDS PAGE. In FIG. 15 it is shown that particles are able to protect lysozyme from degradation even in its reduced and alkylated form.

In order to better understand the mechanism of protection from proteolysis, an experiment was performed with plain particles. NIP Am particles were incubated at 37 C in a pH 7 NH4HC03 (100 mM) solution containing reduced and alkylated lysozyme (0.5 mg/mL) and trypsin (0.05 mg/mL) for one hour. The results are reported in FIG. 15 and show products of lysozyme degradation inside the particles. This suggests that the AAc bait plays a fundamental role in protecting proteins from degradation.

The development and application of hydrogel bait-containing particles as a new tool for harvesting and concentrating small molecule analytes and biomarker candidates from biological fluids has been described, allowing high throughput analysis of low abundance and low molecular weight components. These nanoparticles present a rapid and straightforward workflow for direct utility in raw body fluids, while the work herein described the particles with a negative charge that preferentially bind cationic species, positively charged particles such as a NIP Ami allylamine copolymer could be used to selectively harvest and concentrate anionic species from biological fluids. Similarly, hydrophobic metabolites could be captured for comprehensive metabolomic studies by using more hydrophobic particles such as NIP AmIstyrene copolymers. Analyte-specific chemical or protein or nucleic acid affinity baits can be incorporated. For example, boronate-containing particles, which are known to bind saccharides, would be utilized to sequester glycoproteins from solution (Ivanov et al., Journal of molecular recognition 2006, 19, (4), 322-31). Consequently, NIPAm-allylamine copolymers are currently being synthesized that contain a bait for anionic proteins. Moreover, p-vinylphenylboronic acid (VPBA) is under consideration as a copolymer for harvesting of sugars and nucleic acids. Further affinity baits such as triazinil-based reactive dyes (that have affinity towards proteins), hexadecylamine (for lipids uptake) and cyclodextrins (able to associate small molecules) are being noncovalently or covalently immobilized within the particles. In particular the bait chemistry described above has been used to harvest the following small metabolites L-Dopa, homogentisic acid, Dopamine, Dopac and 5-hydroxyindoleacetic acid. This extends the utility of the technology to the realm of metabolomics.

Combining a variety of affinity chemistries with a size-sieving tool in a one-step process could have enormous utility for disease marker discovery and analysis workflows.

In the workflow presented in this study, proteins are denatured when eluted out of particles and then analyzed in mass spectrometry for biomarker discovery. Nevertheless, it is important to note that the harvesting conditions are conducted with native protein mixtures. This permits future applications that require the analytes of interest to be in their native state (immulite, radioimmunoassays). For these applications it would important that proteins are not denatured when released from the particles. Ahmad and colleagues have demonstrated, using circular dichroism, that molecules for drug delivery released from NiPam particles by temperature changes retained their native conformational state (Ahmad et al., Colloid & Polymer Science 2002, 280, (4), 310-315). Consequently possible means of eluting native proteins from the particles include modifying the temperature or pH of the solution, increasing the ionic strength, or electro eluting the proteins under non denaturing conditions, in the absence of detergent.

Example 12 NIPAmJAAc Core NIPAm Shell Particles Synthesis

In this particle architecture, a core, containing affinity bait moieties, is surrounded by a NIP Am shell. The sieving capability of the NIP Am shell will shield the core and its affinity bait groups from larger molecules that may be present and could compete with the intended low-abundance low molecular weight molecular targets for binding to the affinity bait in the core. A shell solution was prepared by dissolving NIP Am, 0.02 molar equivalents each of BIS and SDS in H20 and filtering the solution through a membrane filter. The solution was degassed under vacuum for several minutes and then purged with nitrogen for 2 h at room temperature with stirring. While the shell solution was purged, the core solution was prepared by dissolving NIPAm, 0.08 molar equivalents of Mc and 0.02 molar equivalents of BIS in H20 and then the solution was filtered. The core solution was then degassed and purged with nitrogen at 70° C. as described for the preparation of the NIP Am particles. Once the solution had equilibrated at 70° C. and stirred under nitrogen for 1 hour, APS (0.005 molar equivalents) was added, to the core solution. After the NIP Aml AAc core reaction had been allowed to incubate for 3 h at 70° C. under nitrogen, the shell solution was added to the reaction flask followed by and additional aliquot of APS. The reaction was then allowed to stir at 70° C. under nitrogen for an additional 3 h. At which point, the reaction was removed from heat and allowed to stir overnight under nitrogen at room temperature. The particles were then collected and washed in the same fashion as described for the NIP Am particles.

Example 13 Core Shell Particles have the Same Molecular Sieving Cut Off as NIPAmIAAc

Light scattering measurement of core shell particles diameter gave a value of 1048 nm for the NIP Ami AAc core and 1198 nm when the NIP Am shell was added. In order to determine if core shell particles had the same molecular weight cut off (MWCO) as NIP Ami AAc particles, a solution of protein molecular weight markers was used. The solution consisted of 0.5 mg/mL of each of the following proteins: aprotinin (MW 6,500 Da, Sigma-Aldrich), lysozyme (MW 14,400 Da, Sigma-Aldrich), trypsin inhibitor (MW 21,500 Da, Invitrogen), carbonic anhydrase (MW 31,000 Da, Sigma-Aldrich), ovalbumin (MW 45,000 Da, Sigma-Aldrich), and BSA (MW 66,000 Da, Fisher Scientific) dissolved in Tris (pH 7, 50 mM). Incubation time was 1 hour and particles were washed as described in the manuscript. SDS PAGE analysis reported in FIG. 16 shows a substantial agreement in MWCO values for the two types of particles.

Example 14 Core Shell Particles Protect Lysozyme from Chymotrypsin Enzymatic Degradation

Another protease, a-chymotrypsin (MW 25,000 Da, pl=8.75, Sigma), was chosen to prove the ability of particles to protect proteins from degradation. achymotrypsin was used at a ratio of 1:10 (w/w) for a-chymotrypsin:lysozyme. Lysozyme digestion was performed in 100 mM Tris HCl containing 10 mM CaCl2, pH 7.8, at 30° C. for 3 hours. Core shell particles were incubated with lysozyme and trypsin in the digestion conditions described above. Also in this case, particles protected lysozyme from chymotrypsin degradation (FIG. 17, lane 5). Lysozyme degradation is also evident in the incubation without particles (FIG. 17, lane 3).

We developed a core-shell particle in which a N-isopropylacrylamide (NIP Am)Acrylic acid (Mc) core contains a charge based bait to perform affinity binding to proteins in solutions, and a NIP Am shell surrounds the core and acts as a sieve to exclude solution phase proteins too large to penetrate the porosity of the shell (Scheme 1). Because of their porous structure, NIP Am based particles are perfect candidates to exclude larger molecules. The degree of porosity can be tuned by changing the percentage of cross-linker N,N′ methylenebisacrylamide (BIS) with respect to the monomer. At the same time, particles can imbibe large amounts of water which provide favorable conditions for polypeptides and other small molecules to penetrate the polymer matrix, and also allowing concentration of rare protein biomarkers. [14] We envision the introduction of hydrogel particles directly in a blood or body fluid sample where they will remove all of their target molecules, in one step, in solution, from the entire volume of the sample and concentrate the sequestered analytes inside the particles. Analytes will be then drawn out from the particles in a very small volume to yield a much higher concentration per volume of the size fractionated analyte compared to the starting sample. Depending on the starting volume, this technology has the potential to achieve many hundred-fold concentration of the biomarker, with preservation against degradation, within minutes. This is because the starting volume of a blood or urine sample is usually much larger (e.g. 5 mL) compared to the 10 to 50 microliters that is used for a routine clinical assay, gel electrophoresis, or mass spectrometry. Employing particle capture, all of the analyte within the 5 mL can be theoretically captured, separated from the vast overabundance of resident proteins in the starting sample, and then eluted into a small assay volume.

In order to study the applicability of hydrogel particles to a real world problem PDGF was chosen as a highly challenging model for cancer related biomarker analysis because it is present in blood in extremely low concentration (3 ng mL-1), with a short half life (2 minutes). [12] The PDGFs are a family of peptide growth factors that signal through cell surface tyrosine kinase receptors and stimulate various cellular functions including growth, proliferation, and differentiation. Four different polypeptide chains (PDGF-A, -B, -C, and -D) encoded by different genes (chromosomes 4, 7, 11, 22) have been described. [22,23] PDGF plays a role in angiogenesis and the level of tumor interstitial pressure during tumor progression. [24-26] Several new therapeutic agents designed to target PDGF and its receptor are presently in use in the oncology clinic.[27-31] Despite this known theranostic value, PDGF can not be measured routinely and accurately in the clinic because of the extreme low abundance and high instability of this low molecular weight growth factor.

In this paper, we apply (NIP Ami AAc) core-(NIPAm) shell nanoparticles to amplifY the concentration of PDGF, stabilize PDGF, and exclude contaminating carrier proteins such as albumin as a model for the practical application of core shell harvesting particles to analysis of low abundant, low molecular weight, and labile cancer biomarkers.

2. Results and Discussion

2.1. Particles Synthesis and Characterization

For the particle architecture used in the present study, a NIPAm shell surrounds a NIPAmIAAc core, containing affinity bait moieties. The sieving capability of the NIPAm shell shields the core and its affinity bait groups from larger molecules that may be present and could compete with the intended low-abundance, low molecular weight molecular targets for binding to the affinity bait in the core. Light scattering characterization was conducted on particles during the synthesis process and at the end of the process in order to compare the sizes of the core and the core shell particles. Results are reported in FIG. 18, and show that the core diameter at 25° C. and pH 4.5 is 364.7+/−4.3 nm whereas the diameter of the core-shell particles at the same conditions is 699.4+/−6.2 nm. This suggests that the thickness of the shell is about 170 nm. As is characteristic behavior of AAc containing hydro gels, core shell particles size decreased with increasing temperature and decreasing pH. Particles were further characterized by means of atomic force microscopy. AFM images of these particles (FIG. 18) showed size homogeneity, and particle diameters readings were consistent with those measured with light scattering.

2.2. Molecular Sieving and Concentration of PDGF by Core Shell Particles

Human platelet derived growth factor (PDGF, MW 14,500 Da) was chosen as a significant model for serological cancer biomarkers and was studied in a solution containing bovine serum albumin (BSA, MW 66,000 Da) as carrier protein associated with the PDGF. 50 f.ll of a solution containing 0.02 mg mL-1 PDGF, 0.2 mg mL-1 BSA in 50 mM TrisHCl pH 7 was incubated with 50 f.ll of core shell particles and washed with water. Particles and supernatant were analyzed by 1-D gel electrophoresis (SDS-PAGE). The particles were retained in the stacking region of the gel while all of the captured proteins were electroeluted from particles and resolved in the gel. There was no detectable association of BSA with the particles, and the particles completely sequestered all the solution phase PDGF while completely excluding the BSA (FIG. 19). This suggests that PDGF affinity for the bait was higher than that for carrier BSA. In order to further assess the molecular sieving properties of particles, 50 f.ll of core shell particles were incubated for 30 minutes with 50 f.ll of a solution containing proteins with a broad range of molecular weight. The solution contained the following proteins: PDGF, BSA, aprotinin (MW 6,500 Da), lysozyme (MW 14,400 Da), trypsin inhibitor (MW 21,500 Da), carbonic anhydrase (MW 31,000 Da), and ovalbumin (MW 45,000 Da), each at a concentration of 0.05 mg mL-1 dissolved in 50 mM Tris pH 7. The uptake of proteins was evaluated by SDS PAGE. Core shell particles efficaciously captured and concentrated low molecular weight proteins with a weight less than 21,500 Da whereas proteins with high molecular weight remained excluded from the particles (FIG. 19).

One of the key problems for biomarker discovery, validation and routine clinical measurement is the extreme low concentration of biomarkers in biological fluids, often below the detection limit of current measurement technologies. A commercial clinical grade ELISA platform was used to study the core-shell particles ability to raise the concentration of extremely dilute undetectable analytes into the detection range of the assay. Thus we examined the nanoparticles ability to concentrate a dilute PDGF sample, at a concentration below the detection threshold of the ELISA, to determine if the concentration of PDGF could be increased particle sequestration, rendering the PDGF measurable by the ELISA.

Human PDGF-BB ELISA was performed according to manufacturer's instructions. Each measurement was carried out in duplicate and individual standard curves were generated for each set of samples assayed. Aliquots of 1 ml of PDGF solution below the detection limit of the kit (20 pg mL-1) were incubated for 30 minutes with different numbers of particles (50, 100, 200, and 500 f.ll). Proteins were eluted from the washed particles by means of two subsequent elution steps with 60% acetonitrile and 2% acetic acid. ELISA readings were performed on a volume of 100 f.ll. As shown in FIG. 20, previously undetectable levels of PDGF was recovered from the particles and successfully quantified by ELISA at concentrations ranging from 75 to 102 pg mL-1. Therefore, core shell particles, incubated with a PDGF solution at a concentration undetectable by ELISA, harvested and concentrated PDGF to a level higher than the detection limit of the assay. The saturation curve presented in FIG. 20 insert demonstrated that saturation was reached with the minimum amount of particles when the PDGF solution was very dilute. In FIG. 20, readings from a similar experiment performed with a more concentrated PDGF solution are reported. The concentration of PDGF in the starting solution was 63.69 (+/−1.448) pg mL-1 whereas the concentration of PDGF recovered from particles was 452.81 (+/−4.818) pg mL-1 yielding a concentration factor of about 7 over the theoretical of 10. Results from incubations of PDGF solution with different volumes of particles are shown in FIG. 20, insert, and demonstrated that saturation was reached when the volume of particles was 200 f.ll (46 million particles, 1:5 v/v particles:PDGF solution ratio).

2.3. Protection from Enzymatic Degradation of PDGF by Using Core Shell Particles

Degradation of biomarkers by endogenous and exogenous proteases is a major source of biomarker performance bias, and hinders the discovery and measurement of candidate biomarkers. Western blot analysis was used to evaluate the particles ability to protect PDGF from enzymatic degradation. PDGF-BSA solution (0.11 mg mL-1 total protein) was incubated with trypsin at 1:100 w/w protein:protease ratio for different time periods (0, 10, 20, and 60 minutes) in order to study the degradation patterns over time. Particles then were incubated for 1 hour at 37° C. in a 50 mM TrisHCl pH 7 solution containing PDGF-BSA (0.11 mg mL-1 total protein) and trypsin (0.011 mg mL-1). After incubation, the particles were washed, and subjected to SDS-PAGE. Proteins were transferred onto a polyvinylidene fluoride (PVDF) membrane for immunoblotting. The membrane was stained for total protein and subsequently incubated with anti-PDGF antibody. As shown in FIG. 21, trypsin action on PDGF in the absence of particles was evident after 10 minutes and almost complete after one hour, as indicated by nearly undetectable PDGF bands at 14,000-17,000 Da (Lanes 6-8). In marked contrast, PDGF incubated with trypsin and core shell particles generated a single species band that was not diminished in staining intensity and was not fragmented, suggesting that particles successfully preserved PDGF from proteolysis (Lane 4). The PDGF band for the particles loaded with PDGF without trypsin (Lane 2) was identical to that for the particles loaded with PDGF and trypsin (Lane 4) further suggesting that no PDGF protein was lost because of enzymatic degradation.

2.4. Core Shell Particles Concentrate and Preserve PDGF Spiked in Human Serum

The extremely short half-life of PDGF in plasma, about two minutes, is a major analytical challenge. Immunoblotting and mass spectrometry were used to study the efficiency of core shell particles to harvest, concentrate and preserve PDGF spiked in human serum. Immunoblotting was used to verify the preservation of PDGF by the presence of the correct molecular weight intact protein.

Aliquots of 50 f.ll of core shell particles were incubated with 50 f.ll of a solution where PDGF was spiked in human serum diluted 1:25 in 50 mM TrisHCl pH 7 at a concentration of 5 ng mL-1 or 2 ng mL-1 for 1 hour at room temperature. As shown in FIG. 22, particles excluded the high molecular weight proteins which remained in the supernatant (Lane 2 and Lane 5) and at the same time they concentrated PDGF (Lane 3 and Lane 6) that was spiked in serum at two different concentrations. As shown above with the ELISA, PDGF in the starting solution was undetectable (Lane 1 and 4). Particles increased the concentration of PDGF well above the western blot detection limit within an extraordinarily complex serum solution, with no detectable alteration in the mass or abundance of the molecule.

The present invention is a core-shell particle that is made up of a N-isopropylacrylamide (NIP Am)-Acrylic acid (AAc) core, with the core having a charge based bait configured to perform affinity binding to proteins in solutions. A NIP Am shell surrounds the core and is configured to act as a sieve to exclude solution phase proteins too large to penetrate the porosity of the shell. A cross-linker N,N′ methylenebisacrylamide (BIS) is configured to change with respect to a monomer while particles configured to imbibe large amounts of water provide favorable conditions for polypeptides and other small molecules to penetrate a polymer matrix. The particles also are configured to allow concentration of rare protein biomarkers.

The present invention in an embodiment is a particle for isolating an analyte from a mixture, made up of a polymeric matrix, where the polymeric matrix has a pore size that under certain conditions allows for the analyte to enter the polymeric matrix while excluding other compounds from the mixture from entering the polymeric matrix. The analyte is selected from the group consisting of: metabolites, proteins, RNA, micro RNA, DNA, glycoproteins, lipids, glycolipids, proteolipids, hormones, cytokines, growth factors, biomarkers, drug compounds, synthetic organic compounds, volatile odorants, toxicants and pollutants. The polymeric matrix is expandable and contractible, although an additional embodiment is such where this is not the case. When the polymeric matrix expands or contracts, the pore size of the gel matrix expands or contracts, respectively. It also should be noted that the polymeric matrix is expandable and contractible in response to an applied stimulus, which is a thermal, electrical, magnetic, ultrasound, pressure, radiant, laser, osmotic, or pH change. The polymeric matrix is expandable or contractible also upon treatment with an enzyme. The present invention also comprises an attractant that is sequestered with the capture particle. The attractant is covalently bonded to the capture particle, with the attractant being integrated into the polymeric matrix. The attractant also can be deemed to be an affinity ligand, wherein the affinity ligand comprises an antibody or protein, an aptamer, nucleic acid, a drug, a chemical, a metabolite, a lipid, a glycolipid, a phospholipid, a polypeptide, an affinity group, or a metal group. In addition, the present invention includes a detectable label.

The present invention also employs a core-shell particle, the core-shell particle consisting of a N-isopropyl a cry lamide (NIPAm)-Acrylic acid (Mc) core, with the core having a charge based bait configured to perform affinity binding to proteins in solutions. A NIP Am shell surrounds the core and is configured to act as a sieve to exclude solution phase proteins too large to penetrate the porosity of the shell, a cross-linker N,N′methylenebisacrylamide (BIS) configured to change with respect to a monomer, and particles configured to imbibe large amounts of water which provide favorable conditions for polypeptides and other small molecules to penetrate a polymer matrix. It is important to add that the particles also are configured in this embodiment to allow concentration of rare protein biomarkers.

A capture particle for isolating an analyte from a mixture also is part of the present invention, comprising a co-polymeric matrix comprising a structural monomer and an affinity monomer. The polymeric matrix has a pore size that under certain conditions allows for the analyte to enter the polymeric matrix while excluding other compounds from the mixture from entering the polymeric matrix. The analyte is selected from the group consisting of: metabolites, proteins, RNA, micro RNA, DNA, glycoproteins, lipids, glycolipids, proteolipids, hormones, cytokines, growth factors, biomarkers, drug compounds, synthetic organic compounds, volatile odorants, toxicants and pollutants. The capture particle has a molecular weight cutoff size of about 5 to about 100 kDa or 20 to about 50 kDa. The structural monomer is selected from the group consisting of: acrylamide and derivatives thereof, N-alkyl substituted acrylamides, N,N methylenebisacrylamide, N,N-cystaminebisacrylamide, N-vinylalkylamides, acrylic acid, methacrylic acid, allylamine, styrene, benzyl glutamate, 2-ethylacrylic acid, 4-vinylpyridine, silicone, hydroxyethyl methacrylate, ethylene oxide, butylenes terephthalate, 2-acrylamido-2-methyl-1-propanesulfonic acid, vinylpyrrolidone, ethylenevinyl acetate, lactide, glycolide, caprolactone, hydroxyalkanoate, chitosan, hyaluronic acid, starch, cellulose and agarose. The structural monomer is N-isopropylacrylic acid. The affinity monomer comprises a positively charged moiety, with the positively charged moiety being selected from the group consisting of: amine groups and amide groups. The affinity monomer comprises a negatively charged moiety, with the negatively charged moiety being selected from the group consisting of: carboxylic acid groups, hydroxyl groups, thiol groups and phosphate groups. The affinity monomer is selected from the group consisting of: affinity dyes, boronic acid groups, nucleic acids, glycopeptides, glycoproteins, cyclodextrins, calixarenes, porphyrin groups, and aliphatic groups. As mentioned above, the affinity monomer is acrylic acid. The embodiment of the present invention employs a core-shell particle, the core-shell particle comprising a Nisopropylacrylamide (NIP Am)-Acrylic acid (AAc) core. The core has a charge based bait configured to perform affinity binding to proteins in solutions while a NIP Am shell surrounds the core and is configured to act as a sieve to exclude solution phase proteins too large to penetrate the porosity of the shell. The cross-linker N,N′ methylenebisacrylamide (BIS) is configured to change with respect to a monomer. Particles configured to imbibe large amounts of water provide favorable conditions for polypeptides and other small molecules to penetrate a polymer matrix. The particles also are configured to allow concentration of rare protein biomarkers.

The present invention also features an embodiment as a method for harvesting nanoparticles to the assay of platelet derived growth factor. This is comprised of introducing hydrogel particles directly in a body fluid sample, allowing the hydrogel particles to remove all target molecules, in one step, in solution, from an entire volume of the sample and concentrating sequestered analytes inside the hydrogel particles. Analytes are drawn out from the hydrogel particles in a very small volume to yield a much higher concentration per volume of size fractionated analytes compared to the sample.

An additional embodiment of the present invention relates to a protocol that synthesizes the NIP Ami AAc core-shell particles. Materials used for this additional embodiment are N-Isopropylacrylamide (NIPAm), N—N′-methylenebis(acrylamide) (BIS), ammonium persulfate (APS) and acrylic acid (AAc). Water for all reactions, solution preparation, and polymer washing are distilled, purified with a Millipore Milli-Q water purification system to a resistance of 18 M and passed through a 0.2 m filter. NIPAm (8.84 mmol), BIS (0.18 mmol) is dissolved in 30 mL of H20 and then filtered once through a membrane filter and degassed for 15 min. The solution is then purged with nitrogen for 2 h at room temperature and medium stir rate. The core solution is prepared by dissolving NIP Am (8.13 mmol), BIS (0.18 mmol), and Mc (0.706 mmol) in 30 mL of H20 and then filtered in the same manner as above. The solution is transferred into a 250 mL three-neck, round-bottom flask and heated under a constant nitrogen stream until a stable temperature of 70° C. is achieved. A 1.0 mL aqueous solution of APS (0.0433 mmol) is then added to the reaction flask to initiate polymerization. After incubating the p-NIPAm-co-AAc core solution for 3 h at 70 C with medium stirring under nitrogen, the degassed shell solution is added in a dropwise fashion to the reaction flask with the aid of an addition funnel. The reaction is stirred at a medium stir rate qt C under nitrogen for a 3 h period beginning at the initiation of addition of the shell solution. At which point, the reaction is allowed to cool to room temperature overnight under a constant nitrogen stream. The particles are pelleted via centrifugation (Eppendorf 5415R centrifuge) for 20 minutes at 23 C and 13,000 ref. The supernatant was discarded and the pellets are resuspended in dH20. This step is repeated four more times to wash the particles of any unreacted monomers. After the final centrifugation redispersion step is completed, the supernatant is discarded and the washed particles is resuspended in dH20 for storage. 

What is claimed is:
 1. A capture particle for isolating an analyte from a mixture, comprising: a co-polymeric matrix comprising a structural monomer and an affinity monomer; wherein the polymeric matrix has a pore size that under certain conditions allows for the analyte to enter the polymeric matrix while excluding other compounds from the mixture from entering the polymeric matrix; wherein the analyte is selected from the group consisting of: metabolites, proteins, RNA, micro RNA, DNA, glycoproteins, lipids, glycolipids, proteolipids, hormones, cytokines, growth factors, biomarkers, drug compounds, synthetic organic compounds, volatile odorants, toxicants and pollutants; and wherein the structural monomer is Nisopropylacrylic acid.
 2. A capture particle for isolating an analyte from a mixture, comprising: a co-polymeric matrix comprising a structural monomer and an affinity monomer; wherein the polymeric matrix has a pore size that under certain conditions allows for the analyte to enter the polymeric matrix while excluding other compounds from the mixture from entering the polymeric matrix; wherein the analyte is selected from the group consisting of: metabolites, proteins, RNA, micro RNA, DNA, glycoproteins, lipids, glycolipids, proteolipids, hormones, cytokines, growth factors, biomarkers, drug compounds, synthetic organic compounds, volatile odorants, toxicants and pollutants; and wherein the affinity monomer is selected from the group consisting of: affinity dyes, boronic acid groups, nucleic acids, glycopeptides, glycoproteins, cyclodextrins, calixarenes, porphyrin groups, and aliphatic groups. 